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rs63750458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs63750458(G;G)
Make rs63750458(G;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47408552
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750458
ebirs63750458
HLIrs63750458
Exacrs63750458
Varsomers63750458
Maprs63750458
PheGenIrs63750458
hapmaprs63750458
1000 genomesrs63750458
hgdprs63750458
ensemblrs63750458
gopubmedrs63750458
geneviewrs63750458
scholarrs63750458
googlers63750458
pharmgkbrs63750458
gwascentralrs63750458
openSNPrs63750458
23andMers63750458
23andMe allrs63750458
SNP Nexus

SNPshotrs63750458
SNPdbers63750458
MSV3drs63750458
GWAS Ctlgrs63750458
Max Magnitude0
ClinVar
Risk rs63750458(G;G)
Alt rs63750458(G;G)
Reference rs63750458(T;T)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47635691T>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076572.2,