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rs63750936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750936(C;T)
Make rs63750936(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463121
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750936
ebirs63750936
HLIrs63750936
Exacrs63750936
Varsomers63750936
Maprs63750936
PheGenIrs63750936
hapmaprs63750936
1000 genomesrs63750936
hgdprs63750936
ensemblrs63750936
gopubmedrs63750936
geneviewrs63750936
scholarrs63750936
googlers63750936
pharmgkbrs63750936
gwascentralrs63750936
openSNPrs63750936
23andMers63750936
23andMe allrs63750936
SNP Nexus

SNPshotrs63750936
SNPdbers63750936
MSV3drs63750936
GWAS Ctlgrs63750936
Max Magnitude0
ClinVar
Risk rs63750936(T;T)
Alt rs63750936(T;T)
Reference rs63750936(C;C)
Significance Pathogenic
Disease Lynch syndrome Hereditary cancer-predisposing syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.47690260C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076173.2, RCV000129104.2,