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rs63750037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750037(C;T)
Make rs63750037(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47410274
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750037
ebirs63750037
HLIrs63750037
Exacrs63750037
Varsomers63750037
Maprs63750037
PheGenIrs63750037
hapmaprs63750037
1000 genomesrs63750037
hgdprs63750037
ensemblrs63750037
gopubmedrs63750037
geneviewrs63750037
scholarrs63750037
googlers63750037
pharmgkbrs63750037
gwascentralrs63750037
openSNPrs63750037
23andMers63750037
23andMe allrs63750037
SNP Nexus

SNPshotrs63750037
SNPdbers63750037
MSV3drs63750037
GWAS Ctlgrs63750037
Max Magnitude0
ClinVar
Risk rs63750037(T;T)
Alt rs63750037(T;T)
Reference rs63750037(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47637413C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076634.2,