rs775766910

Orientation

plus

Stabilized

plus

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

Make rs775766910(A;C)

Make rs775766910(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

119478925

Gene

HSD17B4

is a	snp
is	mentioned by
dbSNP	rs775766910
dbSNP (classic)	rs775766910
ClinGen	rs775766910
ebi	rs775766910
HLI	rs775766910
Exac	rs775766910
Gnomad	rs775766910
Varsome	rs775766910
LitVar	rs775766910
Map	rs775766910
PheGenI	rs775766910
Biobank	rs775766910
1000 genomes	rs775766910
hgdp	rs775766910
ensembl	rs775766910
geneview	rs775766910
scholar	rs775766910
google	rs775766910
pharmgkb	rs775766910
gwascentral	rs775766910
openSNP	rs775766910
23andMe	rs775766910
SNPshot	rs775766910
SNPdbe	rs775766910
MSV3d	rs775766910
GWAS Ctlg	rs775766910

Max Magnitude

0

ClinVar
Risk	rs775766910(C;C) rs775766910(G;G)
Alt	rs775766910(C;C) rs775766910(G;G)
Reference	Rs775766910(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	HSD17B4
CLNDBN	not provided
Reversed	0
HGVS	NC_000005.9:g.118814620A>G
CLNSRC
CLNACC	RCV000171385.1,