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Links from MedGen

Items: 52

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNAS
(R169H +5 more)
Single nucleotide variant
(missense variant +1 more)
Pseudopseudohypoparathyroidism
+8 more
GUncertain significance
GNAS
Single nucleotide variant
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
Progressive osseous heteroplasia
+9 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
GNAS-related disorder
+9 more
GLikely benign
GNAS
Deletion
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GBenign/Likely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(intron variant)
Pseudohypoparathyroidism type 1C
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism type 1C
+9 more
GLikely benign
GNAS
(E109K +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+8 more
GUncertain significance
GNAS
(S363L)
Single nucleotide variant
(genic upstream transcript variant +3 more)
not provided
+8 more
GUncertain significance
GNAS
Single nucleotide variant
(synonymous variant +1 more)
not provided
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism type 1C
+8 more
GBenign/Likely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
McCune-Albright syndrome
+9 more
GLikely benign
GNAS, GNAS-AS1
Single nucleotide variant
(5 prime UTR variant +1 more)
McCune-Albright syndrome
+8 more
GBenign/Likely benign
GNAS
(Q31*)
Single nucleotide variant
(nonsense +1 more)
Pseudohypoparathyroidism type 1C
+8 more
GPathogenic
GNAS
(G270R +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+8 more
GUncertain significance
GNAS
(P414R)
Single nucleotide variant
(missense variant +2 more)
Pseudohypoparathyroidism type 1C
+8 more
GBenign/Likely benign
GNAS
(E52K)
Single nucleotide variant
(5 prime UTR variant +2 more)
GNAS-related disorder
+9 more
GConflicting classifications of pathogenicity
GNAS
(Q403P)
Single nucleotide variant
(missense variant +2 more)
GNAS-related disorder
+9 more
GLikely benign
GNAS
(G315C +1 more)
Single nucleotide variant
(missense variant +1 more)
Pseudohypoparathyroidism type 1C
+8 more
GUncertain significance
GNAS
(Q180*)
Single nucleotide variant
(synonymous variant +2 more)
GNAS-related disorder
+8 more
GUncertain significance
GNAS
(A426P)
Single nucleotide variant
(genic upstream transcript variant +3 more)
Pseudohypoparathyroidism type 1C
+8 more
GConflicting classifications of pathogenicity
GNAS
(P379L)
Single nucleotide variant
(missense variant +2 more)
Pseudohypoparathyroidism type 1C
+7 more
GUncertain significance
GNAS
(V58fs +5 more)
Duplication
(frameshift variant +1 more)
Pseudohypoparathyroidism type 1B
+8 more
GPathogenic
GNAS
(R172C +5 more)
Single nucleotide variant
(missense variant +1 more)
Pseudohypoparathyroidism type 1B
+11 more
GPathogenic/Likely pathogenic
GNAS
(P345R)
Single nucleotide variant
(missense variant +2 more)
McCune-Albright syndrome
+8 more
GBenign/Likely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism type 1B
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
ACTH-independent macronodular adrenal hyperplasia 1
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
GNAS-related disorder
+10 more
GBenign/Likely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism
+10 more
GBenign/Likely benign
GNAS
(D320N)
Single nucleotide variant
(genic upstream transcript variant +3 more)
not provided
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
McCune-Albright syndrome
+9 more
GBenign/Likely benign
GNAS
(S305P)
Single nucleotide variant
(synonymous variant +2 more)
McCune-Albright syndrome
+8 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
GNAS-related disorder
+9 more
GLikely benign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
GNAS-related disorder
+9 more
GLikely benign
GNAS
(A33D)
Single nucleotide variant
(5 prime UTR variant +2 more)
not provided
+9 more
GUncertain significance
GNAS
(P423H)
Single nucleotide variant
(missense variant +2 more)
not provided
+8 more
GBenign/Likely benign
GNAS
(Q12*)
Single nucleotide variant
(nonsense +1 more)
Pseudohypoparathyroidism type 1C
+11 more
GPathogenic
GNAS
(A488T)
Single nucleotide variant
(genic upstream transcript variant +3 more)
McCune-Albright syndrome
+8 more
GConflicting classifications of pathogenicity
GNAS
(R600G)
Single nucleotide variant
(synonymous variant +2 more)
McCune-Albright syndrome
+8 more
GBenign/Likely benign
GNAS
(M162V)
Single nucleotide variant
(synonymous variant +2 more)
McCune-Albright syndrome
+8 more
GBenign/Likely benign
GNAS
(R147S +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+8 more
GLikely benign
GNAS
(L397V +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+9 more
GBenign/Likely benign
GNAS
(P374T +1 more)
Single nucleotide variant
(missense variant +1 more)
McCune-Albright syndrome
+8 more
GBenign
GNAS
Single nucleotide variant
(synonymous variant +1 more)
Pseudohypoparathyroidism type 1B
+8 more
GBenign/Likely benign
GNAS
(D130fs +5 more)
Deletion
(frameshift variant +1 more)
not provided
+13 more
GConflicting classifications of pathogenicity
GNAS
(R201S +5 more)
Single nucleotide variant
(missense variant +1 more)
Polyostotic fibrous dysplasia, somatic, mosaic
+2 more
GPathogenic
GNAS
(R201H +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GPathogenic
GNAS
(R201C +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GPathogenic
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