U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Links from MedGen

Items: 30

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GNA11
Single nucleotide variant
(intron variant)
Autosomal dominant hypocalcemia 2
+2 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(synonymous variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(intron variant)
not provided
+2 more
GLikely benign
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(synonymous variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
(N198H)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GUncertain significance
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GUncertain significance
GNA11
Single nucleotide variant
(intron variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GConflicting classifications of pathogenicity
GNA11
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(intron variant)
Autosomal dominant hypocalcemia 2
+2 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(synonymous variant)
Autosomal dominant hypocalcemia 2
+3 more
GLikely benign
GNA11
Single nucleotide variant
(synonymous variant)
Autosomal dominant hypocalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(intron variant)
Autosomal dominant hypocalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(synonymous variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GLikely benign
GNA11
Single nucleotide variant
(intron variant)
Autosomal dominant hypocalcemia 2
+2 more
GUncertain significance
GNA11
Single nucleotide variant
(synonymous variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GConflicting classifications of pathogenicity
GNA11
(V269I)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GUncertain significance
GNA11
(T96M)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
GNA11
Single nucleotide variant
(synonymous variant)
Familial hypocalciuric hypercalcemia 2
+3 more
GBenign/Likely benign
GNA11
Single nucleotide variant
(synonymous variant)
GNA11-related disorder
+4 more
GLikely benign
GNA11
(R60L)
Single nucleotide variant
(missense variant)
Autosomal dominant hypocalcemia 2
GPathogenic
GNA11
(S211W)
Single nucleotide variant
(missense variant)
Autosomal dominant hypocalcemia 2
GPathogenic
GNA11
(R60C)
Single nucleotide variant
(missense variant)
Familial hypocalciuric hypercalcemia 2
+2 more
GPathogenic/Likely pathogenic
GNA11
(F341L)
Single nucleotide variant
(missense variant)
Autosomal dominant hypocalcemia 2
GPathogenic
GNA11
(R181Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
Format
Items per page
Sort by
Choose Destination