rs796051906

Orientation

plus

Stabilized

plus

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

Make rs796051906(CGC;TGT)

Make rs796051906(TGT;TGT)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

120738874

Gene

ACADS

is a	snp
is	mentioned by
dbSNP	rs796051906
dbSNP (classic)	rs796051906
ClinGen	rs796051906
ebi	rs796051906
HLI	rs796051906
Exac	rs796051906
Gnomad	rs796051906
Varsome	rs796051906
LitVar	rs796051906
Map	rs796051906
PheGenI	rs796051906
Biobank	rs796051906
1000 genomes	rs796051906
hgdp	rs796051906
ensembl	rs796051906
geneview	rs796051906
scholar	rs796051906
google	rs796051906
pharmgkb	rs796051906
gwascentral	rs796051906
openSNP	rs796051906
23andMe	rs796051906
SNPshot	rs796051906
SNPdbe	rs796051906
MSV3d	rs796051906
GWAS Ctlg	rs796051906

Max Magnitude

0

ClinVar
Risk	rs796051906(TGT;TGT)
Alt	rs796051906(TGT;TGT)
Reference	Rs796051906(CGC;CGC)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ACADS
CLNDBN	not provided
Reversed	0
HGVS	NC_000012.11:g.121176677_121176679delCGCinsTGT
CLNSRC
CLNACC	RCV000185708.3,