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rs63750097

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750097(C;T)
Make rs63750097(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414338
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750097
ebirs63750097
HLIrs63750097
Exacrs63750097
Varsomers63750097
Maprs63750097
PheGenIrs63750097
hapmaprs63750097
1000 genomesrs63750097
hgdprs63750097
ensemblrs63750097
gopubmedrs63750097
geneviewrs63750097
scholarrs63750097
googlers63750097
pharmgkbrs63750097
gwascentralrs63750097
openSNPrs63750097
23andMers63750097
23andMe allrs63750097
SNP Nexus

SNPshotrs63750097
SNPdbers63750097
MSV3drs63750097
GWAS Ctlgrs63750097
Max Magnitude0
ClinVar
Risk rs63750097(T;T)
Alt rs63750097(T;T)
Reference rs63750097(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47641477C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076738.2,