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rs10121009

From SNPedia

Orientationplus
Stabilizedplus
Make rs10121009(C;C)
Make rs10121009(C;T)
Make rs10121009(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position35269822
GeneUNC13B
is asnp
is mentioned by
dbSNPrs10121009
ebirs10121009
HLIrs10121009
Exacrs10121009
Varsomers10121009
Maprs10121009
PheGenIrs10121009
hapmaprs10121009
1000 genomesrs10121009
hgdprs10121009
ensemblrs10121009
gopubmedrs10121009
geneviewrs10121009
scholarrs10121009
googlers10121009
pharmgkbrs10121009
gwascentralrs10121009
openSNPrs10121009
23andMers10121009
23andMe allrs10121009
SNP Nexus

SNPshotrs10121009
SNPdbers10121009
MSV3drs10121009
GWAS Ctlgrs10121009
GMAF0.3485
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21812969OA-icon.png]
Trait
Title Genome-Wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.
Risk Allele A
P-val 0.000003
Odds Ratio None None


[PMID 18633107OA-icon.png] G/T substitution in intron 1 of the UNC13B gene is associated with increased risk of nephropathy in patients with type 1 diabetes.