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rs63751079

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs63751079(-;-)
Make rs63751079(-;G)
Make rs63751079(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47478488
GeneMSH2
is asnp
is mentioned by
dbSNPrs63751079
ebirs63751079
HLIrs63751079
Exacrs63751079
Varsomers63751079
Maprs63751079
PheGenIrs63751079
hapmaprs63751079
1000 genomesrs63751079
hgdprs63751079
ensemblrs63751079
gopubmedrs63751079
geneviewrs63751079
scholarrs63751079
googlers63751079
pharmgkbrs63751079
gwascentralrs63751079
openSNPrs63751079
23andMers63751079
23andMe allrs63751079
SNP Nexus

SNPshotrs63751079
SNPdbers63751079
MSV3drs63751079
GWAS Ctlgrs63751079
Max Magnitude0
ClinVar
Risk rs63751079(G;G)
Alt rs63751079(G;G)
Reference rs63751079(;)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47705627dupG
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076472.2,