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rs144809928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs144809928(A;A)
Make rs144809928(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position96235548
GeneHSD17B3
is asnp
is mentioned by
dbSNPrs144809928
dbSNP (old)rs144809928
ClinGenrs144809928
ebirs144809928
HLIrs144809928
Exacrs144809928
Gnomadrs144809928
Varsomers144809928
LitVarrs144809928
Maprs144809928
PheGenIrs144809928
Biobankrs144809928
1000 genomesrs144809928
hgdprs144809928
ensemblrs144809928
gopubmedrs144809928
geneviewrs144809928
scholarrs144809928
googlers144809928
pharmgkbrs144809928
gwascentralrs144809928
openSNPrs144809928
23andMers144809928
23andMe allrs144809928
SNPshotrs144809928
SNPdbers144809928
MSV3drs144809928
GWAS Ctlgrs144809928
Max Magnitude0
ClinVar
Risk rs144809928(A;A)
Alt rs144809928(A;A)
Reference Rs144809928(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HSD17B3
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.98997830G>A
CLNSRC
CLNACC RCV000255975.1,