Have questions? Visit https://www.reddit.com/r/SNPedia

rs63751271

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;C) 6 Lynch syndrome, pathogenic mutation
(C;C) 0 common in clinvar


Make rs63751271(A;A)
ReferenceGRCh38 38.1/141
Chromosome2
Position47429880
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751271
dbSNP (old)rs63751271
ClinGenrs63751271
ebirs63751271
HLIrs63751271
Exacrs63751271
Gnomadrs63751271
Varsomers63751271
Maprs63751271
PheGenIrs63751271
Biobankrs63751271
1000 genomesrs63751271
hgdprs63751271
ensemblrs63751271
gopubmedrs63751271
geneviewrs63751271
scholarrs63751271
googlers63751271
pharmgkbrs63751271
gwascentralrs63751271
openSNPrs63751271
23andMers63751271
23andMe allrs63751271
SNP Nexus

SNPshotrs63751271
SNPdbers63751271
MSV3drs63751271
GWAS Ctlgrs63751271
Max Magnitude6
ClinVar
Risk rs63751271(A;A)
Alt rs63751271(A;A)
Reference Rs63751271(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47657019C>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076063.2,