rs398123094

Merged into

rs387906252

Orientation

plus

Stabilized

plus

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

Make rs398123094(-;-)

Make rs398123094(-;AGA)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7222684

Gene

ACADVL

is a	snp
is	mentioned by
dbSNP	rs398123094
dbSNP (classic)	rs398123094
ClinGen	rs398123094
ebi	rs398123094
HLI	rs398123094
Exac	rs398123094
Gnomad	rs398123094
Varsome	rs398123094
LitVar	rs398123094
Map	rs398123094
PheGenI	rs398123094
Biobank	rs398123094
1000 genomes	rs398123094
hgdp	rs398123094
ensembl	rs398123094
geneview	rs398123094
scholar	rs398123094
google	rs398123094
pharmgkb	rs398123094
gwascentral	rs398123094
openSNP	rs398123094
23andMe	rs398123094
SNPshot	rs398123094
SNPdbe	rs398123094
MSV3d	rs398123094
GWAS Ctlg	rs398123094

Status

Merged into rs387906252

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs398123094(AGA;AGA)
Significance	Other
Disease	Very long chain acyl-CoA dehydrogenase deficiency not provided
Variation	info
Gene	ACADVL
CLNDBN	Very long chain acyl-CoA dehydrogenase deficiency not provided
Reversed	0
HGVS	NC_000017.10:g.7126003_7126005delAGA
CLNSRC	HGMD OMIM Allelic Variant
CLNACC	RCV000001694.5, RCV000077926.4,