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rs9806762

From SNPedia

Orientationplus
Stabilizedplus
Make rs9806762(A;A)
Make rs9806762(A;G)
Make rs9806762(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position88118508
GeneNTRK3
is asnp
is mentioned by
dbSNPrs9806762
ebirs9806762
HLIrs9806762
Exacrs9806762
Varsomers9806762
Maprs9806762
PheGenIrs9806762
hapmaprs9806762
1000 genomesrs9806762
hgdprs9806762
ensemblrs9806762
gopubmedrs9806762
geneviewrs9806762
scholarrs9806762
googlers9806762
pharmgkbrs9806762
gwascentralrs9806762
openSNPrs9806762
23andMers9806762
23andMe allrs9806762
SNP Nexus

SNPshotrs9806762
SNPdbers9806762
MSV3drs9806762
GWAS Ctlgrs9806762
GMAF0.332
Max Magnitude
? (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 0.000007
Odds Ratio None None