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rs1805105

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ReferenceGRCh38 38.1/142
Chromosome16
Position346264
GeneAXIN1
is asnp
is mentioned by
dbSNPrs1805105
dbSNP (old)rs1805105
ClinGenrs1805105
ebirs1805105
HLIrs1805105
Exacrs1805105
Gnomadrs1805105
Varsomers1805105
Maprs1805105
PheGenIrs1805105
Biobankrs1805105
1000 genomesrs1805105
hgdprs1805105
ensemblrs1805105
gopubmedrs1805105
geneviewrs1805105
scholarrs1805105
googlers1805105
pharmgkbrs1805105
gwascentralrs1805105
openSNPrs1805105
23andMers1805105
23andMe allrs1805105
SNP Nexus

SNPshotrs1805105
SNPdbers1805105
MSV3drs1805105
GWAS Ctlgrs1805105
Max Magnitude0

[PMID 25802106] The variations in the AXIN1 gene and susceptibility to cryptorchidism


[PMID 26968103] Genetic polymorphisms in the Wnt/β-catenin pathway genes as predictors of tumor development and survival in patients with hepatitis B virus-associated hepatocellular carcinoma.


ClinVar
Risk rs1805105(C;C)
Alt rs1805105(C;C)
Reference Rs1805105(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene AXIN1
CLNDBN not specified
Reversed 1
HGVS NC_000016.9:g.396264A>G
CLNSRC
CLNACC RCV000456059.1,