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rs63750697

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750697(A;A)
Make rs63750697(A;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47445629
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750697
ebirs63750697
HLIrs63750697
Exacrs63750697
Varsomers63750697
Maprs63750697
PheGenIrs63750697
hapmaprs63750697
1000 genomesrs63750697
hgdprs63750697
ensemblrs63750697
gopubmedrs63750697
geneviewrs63750697
scholarrs63750697
googlers63750697
pharmgkbrs63750697
gwascentralrs63750697
openSNPrs63750697
23andMers63750697
23andMe allrs63750697
SNP Nexus

SNPshotrs63750697
SNPdbers63750697
MSV3drs63750697
GWAS Ctlgrs63750697
Max Magnitude0
ClinVar
Risk rs63750697(A;A)
Alt rs63750697(A;A)
Reference rs63750697(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47672768T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076134.2,