rs368949613

Orientation

plus

Stabilized

plus

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

Make rs368949613(C;T)

Make rs368949613(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

128906220

Gene

ACAD9

is a	snp
is	mentioned by
dbSNP	rs368949613
dbSNP (classic)	rs368949613
ClinGen	rs368949613
ebi	rs368949613
HLI	rs368949613
Exac	rs368949613
Gnomad	rs368949613
Varsome	rs368949613
LitVar	rs368949613
Map	rs368949613
PheGenI	rs368949613
Biobank	rs368949613
1000 genomes	rs368949613
hgdp	rs368949613
ensembl	rs368949613
geneview	rs368949613
scholar	rs368949613
google	rs368949613
pharmgkb	rs368949613
gwascentral	rs368949613
openSNP	rs368949613
23andMe	rs368949613
SNPshot	rs368949613
SNPdbe	rs368949613
MSV3d	rs368949613
GWAS Ctlg	rs368949613

Max Magnitude

0

ClinVar
Risk	rs368949613(T;T)
Alt	rs368949613(T;T)
Reference	Rs368949613(C;C)
Significance	Pathogenic
Disease	Acyl-CoA dehydrogenase family
Variation	info
Gene	ACAD9
CLNDBN	Acyl-CoA dehydrogenase family, member 9, deficiency of
Reversed	0
HGVS	NC_000003.11:g.128625063C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000023865.3, RCV000201722.1,