rs863223873

Orientation

plus

Stabilized

plus

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

Make rs863223873(G;G)

Make rs863223873(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

128896479

Gene

ACAD9

is a	snp
is	mentioned by
dbSNP	rs863223873
dbSNP (classic)	rs863223873
ClinGen	rs863223873
ebi	rs863223873
HLI	rs863223873
Exac	rs863223873
Gnomad	rs863223873
Varsome	rs863223873
LitVar	rs863223873
Map	rs863223873
PheGenI	rs863223873
Biobank	rs863223873
1000 genomes	rs863223873
hgdp	rs863223873
ensembl	rs863223873
geneview	rs863223873
scholar	rs863223873
google	rs863223873
pharmgkb	rs863223873
gwascentral	rs863223873
openSNP	rs863223873
23andMe	rs863223873
SNPshot	rs863223873
SNPdbe	rs863223873
MSV3d	rs863223873
GWAS Ctlg	rs863223873

Max Magnitude

0

ClinVar
Risk	rs863223873(G;G)
Alt	rs863223873(G;G)
Reference	Rs863223873(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACAD9
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.128615322T>G
CLNSRC
CLNACC	RCV000198768.1,