rs786205574

Orientation

plus

Stabilized

plus

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

Make rs786205574(C;G)

Make rs786205574(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

119477434

Gene

HSD17B4

is a	snp
is	mentioned by
dbSNP	rs786205574
dbSNP (classic)	rs786205574
ClinGen	rs786205574
ebi	rs786205574
HLI	rs786205574
Exac	rs786205574
Gnomad	rs786205574
Varsome	rs786205574
LitVar	rs786205574
Map	rs786205574
PheGenI	rs786205574
Biobank	rs786205574
1000 genomes	rs786205574
hgdp	rs786205574
ensembl	rs786205574
geneview	rs786205574
scholar	rs786205574
google	rs786205574
pharmgkb	rs786205574
gwascentral	rs786205574
openSNP	rs786205574
23andMe	rs786205574
SNPshot	rs786205574
SNPdbe	rs786205574
MSV3d	rs786205574
GWAS Ctlg	rs786205574

Max Magnitude

0

ClinVar
Risk	rs786205574(G;G)
Alt	rs786205574(G;G)
Reference	Rs786205574(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HSD17B4
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.118813129C>G
CLNSRC
CLNACC	RCV000171384.1,