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

rs2303426

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2303426(C;G)
Make rs2303426(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position47403411
GeneMSH2
is asnp
is mentioned by
dbSNPrs2303426
ebirs2303426
HLIrs2303426
Exacrs2303426
Varsomers2303426
Maprs2303426
PheGenIrs2303426
hapmaprs2303426
1000 genomesrs2303426
hgdprs2303426
ensemblrs2303426
gopubmedrs2303426
geneviewrs2303426
scholarrs2303426
googlers2303426
pharmgkbrs2303426
gwascentralrs2303426
openSNPrs2303426
23andMers2303426
23andMe allrs2303426
SNP Nexus

SNPshotrs2303426
SNPdbers2303426
MSV3drs2303426
GWAS Ctlgrs2303426
GMAF0.3843
Max Magnitude0

[PMID 21283657OA-icon.png] Gallbladder Cancer Predisposition: A Multigenic Approach to DNA-Repair, Apoptotic and Inflammatory Pathway Genes

ClinVar
Risk rs2303426(A,G;A,G)
Alt rs2303426(A,G;A,G)
Reference rs2303426(C;C)
Significance Probable-non-pathogenic
Disease Lynch syndrome not specified Lynch syndrome I
Variation info
Gene MSH2
CLNDBN Lynch syndrome not specified Lynch syndrome I
Reversed 0
HGVS NC_000002.11:g.47630550C>A; NC_000002.11:g.47630550C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000230066.1, RCV000030249.3, RCV000035360.8, RCV000144620.1,


[PMID 20564624] Polymorphisms in ERCC2, MSH2, and OGG1 DNA repair genes and gallbladder cancer risk in a population of Northern India.