rs1057516991

Orientation

minus

Stabilized

minus

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

Make rs1057516991(-;-)

Make rs1057516991(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

26195122

Gene	GAREM2, HADHA, LOC107985860

is a	snp
is	mentioned by
dbSNP	rs1057516991
dbSNP (classic)	rs1057516991
ClinGen	rs1057516991
ebi	rs1057516991
HLI	rs1057516991
Exac	rs1057516991
Gnomad	rs1057516991
Varsome	rs1057516991
LitVar	rs1057516991
Map	rs1057516991
PheGenI	rs1057516991
Biobank	rs1057516991
1000 genomes	rs1057516991
hgdp	rs1057516991
ensembl	rs1057516991
geneview	rs1057516991
scholar	rs1057516991
google	rs1057516991
pharmgkb	rs1057516991
gwascentral	rs1057516991
openSNP	rs1057516991
23andMe	rs1057516991
SNPshot	rs1057516991
SNPdbe	rs1057516991
MSV3d	rs1057516991
GWAS Ctlg	rs1057516991

Max Magnitude

0

ClinVar
Risk	rs1057516991(-;-)
Alt	rs1057516991(-;-)
Reference	Rs1057516991(C;C)
Significance	Probable-Pathogenic
Disease	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Variation	info
Gene	HADHA
CLNDBN	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Reversed	1
HGVS	NC_000002.11:g.26417991delG
CLNSRC
CLNACC	RCV000410644.1,