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rs63750857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750857(C;T)
Make rs63750857(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480773
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750857
ebirs63750857
HLIrs63750857
Exacrs63750857
Varsomers63750857
Maprs63750857
PheGenIrs63750857
hapmaprs63750857
1000 genomesrs63750857
hgdprs63750857
ensemblrs63750857
gopubmedrs63750857
geneviewrs63750857
scholarrs63750857
googlers63750857
pharmgkbrs63750857
gwascentralrs63750857
openSNPrs63750857
23andMers63750857
23andMe allrs63750857
SNP Nexus

SNPshotrs63750857
SNPdbers63750857
MSV3drs63750857
GWAS Ctlgrs63750857
Max Magnitude0
ClinVar
Risk rs63750857(T;T)
Alt rs63750857(T;T)
Reference rs63750857(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47707912C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076498.2,