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rs63751469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs63751469(A;A)
Make rs63751469(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position47482779
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751469
ebirs63751469
HLIrs63751469
Exacrs63751469
Varsomers63751469
Maprs63751469
PheGenIrs63751469
hapmaprs63751469
1000 genomesrs63751469
hgdprs63751469
ensemblrs63751469
gopubmedrs63751469
geneviewrs63751469
scholarrs63751469
googlers63751469
pharmgkbrs63751469
gwascentralrs63751469
openSNPrs63751469
23andMers63751469
23andMe allrs63751469
SNP Nexus

SNPshotrs63751469
SNPdbers63751469
MSV3drs63751469
GWAS Ctlgrs63751469
Max Magnitude0
ClinVar
Risk rs63751469(A,T;A,T)
Alt rs63751469(A,T;A,T)
Reference rs63751469(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47709918C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076530.2,