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rs63750636

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750636(C;T)
Make rs63750636(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476492
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750636
ebirs63750636
HLIrs63750636
Exacrs63750636
Varsomers63750636
Maprs63750636
PheGenIrs63750636
hapmaprs63750636
1000 genomesrs63750636
hgdprs63750636
ensemblrs63750636
gopubmedrs63750636
geneviewrs63750636
scholarrs63750636
googlers63750636
pharmgkbrs63750636
gwascentralrs63750636
openSNPrs63750636
23andMers63750636
23andMe allrs63750636
SNP Nexus

SNPshotrs63750636
SNPdbers63750636
MSV3drs63750636
GWAS Ctlgrs63750636
Max Magnitude0
ClinVar
Risk rs63750636(T;T)
Alt rs63750636(T;T)
Reference rs63750636(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome I not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome Lynch syndrome I not provided
Reversed 0
HGVS NC_000002.11:g.47703631C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076405.3, RCV000129341.2, RCV000168732.1, RCV000202062.2,