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rs63750618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750618(A;A)
Make rs63750618(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478395
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750618
ebirs63750618
HLIrs63750618
Exacrs63750618
Varsomers63750618
Maprs63750618
PheGenIrs63750618
hapmaprs63750618
1000 genomesrs63750618
hgdprs63750618
ensemblrs63750618
gopubmedrs63750618
geneviewrs63750618
scholarrs63750618
googlers63750618
pharmgkbrs63750618
gwascentralrs63750618
openSNPrs63750618
23andMers63750618
23andMe allrs63750618
SNP Nexus

SNPshotrs63750618
SNPdbers63750618
MSV3drs63750618
GWAS Ctlgrs63750618
Max Magnitude0
ClinVar
Risk rs63750618(A;A)
Alt rs63750618(A;A)
Reference rs63750618(C;C)
Significance Pathogenic
Disease Lynch syndrome not provided
Variation info
Gene MSH2
CLNDBN Lynch syndrome not provided
Reversed 0
HGVS NC_000002.11:g.47705534C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076458.2, RCV000115517.2,