rs1057517231

Orientation

plus

Stabilized

plus

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

Make rs1057517231(-;-)

Make rs1057517231(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7222784

Gene

ACADVL

is a	snp
is	mentioned by
dbSNP	rs1057517231
dbSNP (classic)	rs1057517231
ClinGen	rs1057517231
ebi	rs1057517231
HLI	rs1057517231
Exac	rs1057517231
Gnomad	rs1057517231
Varsome	rs1057517231
LitVar	rs1057517231
Map	rs1057517231
PheGenI	rs1057517231
Biobank	rs1057517231
1000 genomes	rs1057517231
hgdp	rs1057517231
ensembl	rs1057517231
geneview	rs1057517231
scholar	rs1057517231
google	rs1057517231
pharmgkb	rs1057517231
gwascentral	rs1057517231
openSNP	rs1057517231
23andMe	rs1057517231
SNPshot	rs1057517231
SNPdbe	rs1057517231
MSV3d	rs1057517231
GWAS Ctlg	rs1057517231

Max Magnitude

0

ClinVar
Risk	rs1057517231(-;-)
Alt	rs1057517231(-;-)
Reference	Rs1057517231(T;T)
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.7126103delT
CLNSRC
CLNACC	RCV000410931.1,