rs191468413

Orientation

plus

Stabilized

plus

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

Make rs191468413(A;A)

Make rs191468413(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

5

Position

119525240

Gene

HSD17B4

is a	snp
is	mentioned by
dbSNP	rs191468413
dbSNP (classic)	rs191468413
ClinGen	rs191468413
ebi	rs191468413
HLI	rs191468413
Exac	rs191468413
Gnomad	rs191468413
Varsome	rs191468413
LitVar	rs191468413
Map	rs191468413
PheGenI	rs191468413
Biobank	rs191468413
1000 genomes	rs191468413
hgdp	rs191468413
ensembl	rs191468413
geneview	rs191468413
scholar	rs191468413
google	rs191468413
pharmgkb	rs191468413
gwascentral	rs191468413
openSNP	rs191468413
23andMe	rs191468413
SNPshot	rs191468413
SNPdbe	rs191468413
MSV3d	rs191468413
GWAS Ctlg	rs191468413

Max Magnitude

0

ClinVar
Risk	rs191468413(A;A)
Alt	rs191468413(A;A)
Reference	Rs191468413(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HSD17B4
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.118860935G>A
CLNSRC
CLNACC	RCV000414223.1,