rs796051913

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGG;AGG)	0	common in clinvar
(GAG;GAG)	0	common in clinvar
(I;I)	0	common genotype

Make rs796051913(-;-)

Make rs796051913(-;GAG)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

7222253

Gene

ACADVL

is a	snp
is	mentioned by
dbSNP	rs796051913
dbSNP (classic)	rs796051913
ClinGen	rs796051913
ebi	rs796051913
HLI	rs796051913
Exac	rs796051913
Gnomad	rs796051913
Varsome	rs796051913
LitVar	rs796051913
Map	rs796051913
PheGenI	rs796051913
Biobank	rs796051913
1000 genomes	rs796051913
hgdp	rs796051913
ensembl	rs796051913
geneview	rs796051913
scholar	rs796051913
google	rs796051913
pharmgkb	rs796051913
gwascentral	rs796051913
openSNP	rs796051913
23andMe	rs796051913
SNPshot	rs796051913
SNPdbe	rs796051913
MSV3d	rs796051913
GWAS Ctlg	rs796051913

Max Magnitude

0

ClinVar
Risk	rs796051913(-;-) Rs796051913(AGG;AGG)
Alt	rs796051913(-;-) Rs796051913(AGG;AGG)
Reference	Rs796051913(GAG;GAG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ACADVL
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.7125572_7125574delGAG
CLNSRC
CLNACC	RCV000185735.3,