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rs2066479

From SNPedia

Orientationminus
Stabilizedminus
Make rs2066479(A;A)
Make rs2066479(A;G)
Make rs2066479(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position96235528
GeneHSD17B3
is asnp
is mentioned by
dbSNPrs2066479
ClinGenrs2066479
ebirs2066479
HLIrs2066479
Exacrs2066479
Varsomers2066479
Maprs2066479
PheGenIrs2066479
hapmaprs2066479
1000 genomesrs2066479
hgdprs2066479
ensemblrs2066479
gopubmedrs2066479
geneviewrs2066479
scholarrs2066479
googlers2066479
pharmgkbrs2066479
gwascentralrs2066479
openSNPrs2066479
23andMers2066479
23andMe allrs2066479
SNP Nexus

SNPshotrs2066479
SNPdbers2066479
MSV3drs2066479
GWAS Ctlgrs2066479
GMAF0.1171
Max Magnitude

[PMID 23139742OA-icon.png] Functional analyses of endometriosis-related polymorphisms in the estrogen synthesis and metabolism-related genes

? (A;A) (A;G) (G;G)
[PMID 19168589OA-icon.png] Variants in hormone-related genes and the risk of biliary tract cancers and stones: a population-based study in China.


ClinVar
Risk rs2066479(A;A) rs2066479(C;C) rs2066479(T;T)
Alt rs2066479(A;A) rs2066479(C;C) rs2066479(T;T)
Reference rs2066479(G;G)
Significance Probable-non-pathogenic
Disease not specified 17-Beta-Hydroxysteroid Dehydrogenase III Deficiency
Variation info
Gene HSD17B3
CLNDBN not specified 17-Beta-Hydroxysteroid Dehydrogenase III Deficiency
Reversed 1
HGVS NC_000009.11:g.98997810C>T
CLNSRC
CLNACC RCV000249456.1, RCV000334343.1,