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rs82625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs82625(A;A)
Make rs82625(A;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position113996371
is asnp
is mentioned by
dbSNPrs82625
ebirs82625
HLIrs82625
Exacrs82625
Varsomers82625
Maprs82625
PheGenIrs82625
hapmaprs82625
1000 genomesrs82625
hgdprs82625
ensemblrs82625
gopubmedrs82625
geneviewrs82625
scholarrs82625
googlers82625
pharmgkbrs82625
gwascentralrs82625
openSNPrs82625
23andMers82625
23andMe allrs82625
SNP Nexus

SNPshotrs82625
SNPdbers82625
MSV3drs82625
GWAS Ctlgrs82625
GMAF0.06703
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22388998OA-icon.png]
Trait
Title Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.
Risk Allele
P-val 0.000002
Odds Ratio None None