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rs63750881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63750881(A;C)
Make rs63750881(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47412504
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750881
ebirs63750881
HLIrs63750881
Exacrs63750881
Varsomers63750881
Maprs63750881
PheGenIrs63750881
hapmaprs63750881
1000 genomesrs63750881
hgdprs63750881
ensemblrs63750881
gopubmedrs63750881
geneviewrs63750881
scholarrs63750881
googlers63750881
pharmgkbrs63750881
gwascentralrs63750881
openSNPrs63750881
23andMers63750881
23andMe allrs63750881
SNP Nexus

SNPshotrs63750881
SNPdbers63750881
MSV3drs63750881
GWAS Ctlgrs63750881
Max Magnitude0
ClinVar
Risk rs63750881(C,T;C,T)
Alt rs63750881(C,T;C,T)
Reference rs63750881(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47639643A>C; NC_000002.11:g.47639643A>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076695.2, RCV000076696.2,