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rs63750961

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750961(C;C)
Make rs63750961(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47476450
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750961
ebirs63750961
HLIrs63750961
Exacrs63750961
Varsomers63750961
Maprs63750961
PheGenIrs63750961
hapmaprs63750961
1000 genomesrs63750961
hgdprs63750961
ensemblrs63750961
gopubmedrs63750961
geneviewrs63750961
scholarrs63750961
googlers63750961
pharmgkbrs63750961
gwascentralrs63750961
openSNPrs63750961
23andMers63750961
23andMe allrs63750961
SNP Nexus

SNPshotrs63750961
SNPdbers63750961
MSV3drs63750961
GWAS Ctlgrs63750961
Max Magnitude0
ClinVar
Risk rs63750961(C;C)
Alt rs63750961(C;C)
Reference rs63750961(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47703589T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076384.2,