rs1060499596

Orientation

plus

Stabilized

plus

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

Make rs1060499596(-;G)

Make rs1060499596(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

7224380

Gene	ACADVL, MIR324

is a	snp
is	mentioned by
dbSNP	rs1060499596
dbSNP (classic)	rs1060499596
ClinGen	rs1060499596
ebi	rs1060499596
HLI	rs1060499596
Exac	rs1060499596
Gnomad	rs1060499596
Varsome	rs1060499596
LitVar	rs1060499596
Map	rs1060499596
PheGenI	rs1060499596
Biobank	rs1060499596
1000 genomes	rs1060499596
hgdp	rs1060499596
ensembl	rs1060499596
geneview	rs1060499596
scholar	rs1060499596
google	rs1060499596
pharmgkb	rs1060499596
gwascentral	rs1060499596
openSNP	rs1060499596
23andMe	rs1060499596
SNPshot	rs1060499596
SNPdbe	rs1060499596
MSV3d	rs1060499596
GWAS Ctlg	rs1060499596

Max Magnitude

0

ClinVar
Risk	rs1060499596(G;G)
Alt	rs1060499596(G;G)
Reference	Rs1060499596(-;-)
Significance	Probable-Pathogenic
Disease	Very long chain acyl-CoA dehydrogenase deficiency
Variation	info
Gene	ACADVL MIR324
CLNDBN	Very long chain acyl-CoA dehydrogenase deficiency
Reversed	0
HGVS	NC_000017.10:g.7127699dupG
CLNSRC
CLNACC	RCV000477936.1,