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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MSH2
Single nucleotide variant
(5 prime UTR variant +1 more)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
MSH2
(N127S +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH2
(V161I +1 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GConflicting classifications of pathogenicity
MSH2
(N120S)
Single nucleotide variant
(missense variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GPathogenic
MSH2
(Q337* +1 more)
Single nucleotide variant
(nonsense)
Lynch syndrome
GPathogenic
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH2
(L390F +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(synonymous variant)
MSH2-related condition
+5 more
GConflicting classifications of pathogenicity
MSH2
Single nucleotide variant
(intron variant)
Hereditary nonpolyposis colorectal neoplasms
+5 more
GBenign/Likely benign
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(synonymous variant)
Lynch syndrome
GBenign
MSH2
(A636P +1 more)
Single nucleotide variant
(missense variant)
Lynch syndrome
GPathogenic
MSH2
(G669D)
Single nucleotide variant
(missense variant +2 more)
Lynch syndrome
GLikely pathogenic
MSH2
Single nucleotide variant
(intron variant)
Lynch syndrome
GBenign
MSH2
Single nucleotide variant
(synonymous variant)
MSH2-related condition
+5 more
GConflicting classifications of pathogenicity
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