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rs63750276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63750276(G;T)
Make rs63750276(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47414335
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750276
ebirs63750276
HLIrs63750276
Exacrs63750276
Varsomers63750276
Maprs63750276
PheGenIrs63750276
hapmaprs63750276
1000 genomesrs63750276
hgdprs63750276
ensemblrs63750276
gopubmedrs63750276
geneviewrs63750276
scholarrs63750276
googlers63750276
pharmgkbrs63750276
gwascentralrs63750276
openSNPrs63750276
23andMers63750276
23andMe allrs63750276
SNP Nexus

SNPshotrs63750276
SNPdbers63750276
MSV3drs63750276
GWAS Ctlgrs63750276
Max Magnitude0
ClinVar
Risk rs63750276(T;T)
Alt rs63750276(T;T)
Reference rs63750276(G;G)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47641474G>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076737.2, RCV000115545.2,