rs796051898

Orientation

plus

Stabilized

plus

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

Make rs796051898(C;C)

Make rs796051898(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

75733530

Gene

ACADM

is a	snp
is	mentioned by
dbSNP	rs796051898
dbSNP (classic)	rs796051898
ClinGen	rs796051898
ebi	rs796051898
HLI	rs796051898
Exac	rs796051898
Gnomad	rs796051898
Varsome	rs796051898
LitVar	rs796051898
Map	rs796051898
PheGenI	rs796051898
Biobank	rs796051898
1000 genomes	rs796051898
hgdp	rs796051898
ensembl	rs796051898
geneview	rs796051898
scholar	rs796051898
google	rs796051898
pharmgkb	rs796051898
gwascentral	rs796051898
openSNP	rs796051898
23andMe	rs796051898
SNPshot	rs796051898
SNPdbe	rs796051898
MSV3d	rs796051898
GWAS Ctlg	rs796051898

Max Magnitude

0

ClinVar
Risk	rs796051898(C;C)
Alt	rs796051898(C;C)
Reference	Rs796051898(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ACADM
CLNDBN	not provided
Reversed	0
HGVS	NC_000001.10:g.76199215G>C
CLNSRC
CLNACC	RCV000185671.1,