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rs9869263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs9869263(A;G)
Make rs9869263(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position190312891
GeneCLDN1
is asnp
is mentioned by
dbSNPrs9869263
ebirs9869263
HLIrs9869263
Exacrs9869263
Varsomers9869263
Maprs9869263
PheGenIrs9869263
hapmaprs9869263
1000 genomesrs9869263
hgdprs9869263
ensemblrs9869263
gopubmedrs9869263
geneviewrs9869263
scholarrs9869263
googlers9869263
pharmgkbrs9869263
gwascentralrs9869263
openSNPrs9869263
23andMers9869263
23andMe allrs9869263
SNP Nexus

SNPshotrs9869263
SNPdbers9869263
MSV3drs9869263
GWAS Ctlgrs9869263
GMAF0.1823
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 24479816] Polymorphisms in the CLDN1 and CLDN7 genes are related to differentiation and tumor stage in colon carcinoma


ClinVar
Risk rs9869263(G;G)
Alt rs9869263(G;G)
Reference rs9869263(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CLDN1
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.190030680A>G
CLNSRC
CLNACC RCV000175932.1,