rs144809928

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs144809928(A;A)

Make rs144809928(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

96235548

Gene

HSD17B3

is a	snp
is	mentioned by
dbSNP	rs144809928
dbSNP (classic)	rs144809928
ClinGen	rs144809928
ebi	rs144809928
HLI	rs144809928
Exac	rs144809928
Gnomad	rs144809928
Varsome	rs144809928
LitVar	rs144809928
Map	rs144809928
PheGenI	rs144809928
Biobank	rs144809928
1000 genomes	rs144809928
hgdp	rs144809928
ensembl	rs144809928
geneview	rs144809928
scholar	rs144809928
google	rs144809928
pharmgkb	rs144809928
gwascentral	rs144809928
openSNP	rs144809928
23andMe	rs144809928
SNPshot	rs144809928
SNPdbe	rs144809928
MSV3d	rs144809928
GWAS Ctlg	rs144809928

Max Magnitude

0

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,