rs1057516843

Orientation

plus

Stabilized

plus

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

Make rs1057516843(-;T)

Make rs1057516843(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7222784

Gene

ACADVL

is a	snp
is	mentioned by
dbSNP	rs1057516843
dbSNP (classic)	rs1057516843
ClinGen	rs1057516843
ebi	rs1057516843
HLI	rs1057516843
Exac	rs1057516843
Gnomad	rs1057516843
Varsome	rs1057516843
LitVar	rs1057516843
Map	rs1057516843
PheGenI	rs1057516843
Biobank	rs1057516843
1000 genomes	rs1057516843
hgdp	rs1057516843
ensembl	rs1057516843
geneview	rs1057516843
scholar	rs1057516843
google	rs1057516843
pharmgkb	rs1057516843
gwascentral	rs1057516843
openSNP	rs1057516843
23andMe	rs1057516843
SNPshot	rs1057516843
SNPdbe	rs1057516843
MSV3d	rs1057516843
GWAS Ctlg	rs1057516843

Max Magnitude

0

ClinVar
Risk	rs1057516843(T;T)
Alt	rs1057516843(T;T)
Reference	Rs1057516843(-;-)
Significance	Probable-Pathogenic
Disease	Very long chain acyl-CoA dehydrogenase deficiency
Variation	info
Gene	ACADVL
CLNDBN	Very long chain acyl-CoA dehydrogenase deficiency
Reversed	0
HGVS	NC_000017.10:g.7126103dupT
CLNSRC
CLNACC	RCV000409885.1,