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rs63750849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63750849(A;A)
Make rs63750849(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47480816
GeneMSH2
is asnp
is mentioned by
dbSNPrs63750849
ebirs63750849
HLIrs63750849
Exacrs63750849
Varsomers63750849
Maprs63750849
PheGenIrs63750849
hapmaprs63750849
1000 genomesrs63750849
hgdprs63750849
ensemblrs63750849
gopubmedrs63750849
geneviewrs63750849
scholarrs63750849
googlers63750849
pharmgkbrs63750849
gwascentralrs63750849
openSNPrs63750849
23andMers63750849
23andMe allrs63750849
SNP Nexus

SNPshotrs63750849
SNPdbers63750849
MSV3drs63750849
GWAS Ctlgrs63750849
Max Magnitude0
ClinVar
Risk rs63750849(A,T;A,T)
Alt rs63750849(A,T;A,T)
Reference rs63750849(C;C)
Significance Pathogenic
Disease Lynch syndrome Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47707955C>A; NC_000002.11:g.47707955C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076507.2, RCV000144616.1, RCV000076508.2,