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rs63749963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs63749963(-;-)
Make rs63749963(-;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47463141
GeneMSH2
is asnp
is mentioned by
dbSNPrs63749963
ebirs63749963
HLIrs63749963
Exacrs63749963
Varsomers63749963
Maprs63749963
PheGenIrs63749963
hapmaprs63749963
1000 genomesrs63749963
hgdprs63749963
ensemblrs63749963
gopubmedrs63749963
geneviewrs63749963
scholarrs63749963
googlers63749963
pharmgkbrs63749963
gwascentralrs63749963
openSNPrs63749963
23andMers63749963
23andMe allrs63749963
SNP Nexus

SNPshotrs63749963
SNPdbers63749963
MSV3drs63749963
GWAS Ctlgrs63749963
Max Magnitude0
ClinVar
Risk rs63749963(;)
Alt rs63749963(;)
Reference rs63749963(A;A)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690280delA
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076177.2,