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rs17429833

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs17429833(C;G)
Make rs17429833(G;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position190322219
GeneCLDN1
is asnp
is mentioned by
dbSNPrs17429833
dbSNP (classic)rs17429833
ClinGenrs17429833
ebirs17429833
HLIrs17429833
Exacrs17429833
Gnomadrs17429833
Varsomers17429833
LitVarrs17429833
Maprs17429833
PheGenIrs17429833
Biobankrs17429833
1000 genomesrs17429833
hgdprs17429833
ensemblrs17429833
geneviewrs17429833
scholarrs17429833
googlers17429833
pharmgkbrs17429833
gwascentralrs17429833
openSNPrs17429833
23andMers17429833
SNPshotrs17429833
SNPdbers17429833
MSV3drs17429833
GWAS Ctlgrs17429833
Max Magnitude0
? (C;C) (C;G) (G;G) 28


[PMID 25785120OA-icon.png] rs17501976 polymorphism of CLDN1 gene is associated with decreased risk of colorectal cancer in a Chinese population


ClinVar
Risk rs17429833(G;G)
Alt rs17429833(G;G)
Reference Rs17429833(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene CLDN1
CLNDBN not specified
Reversed 0
HGVS NC_000003.11:g.190040008C>G
CLNSRC
CLNACC RCV000251825.2,