rs869312991

Orientation

plus

Stabilized

plus

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

Make rs869312991(A;A)

Make rs869312991(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

66088850

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs869312991
dbSNP (classic)	rs869312991
ClinGen	rs869312991
ebi	rs869312991
HLI	rs869312991
Exac	rs869312991
Gnomad	rs869312991
Varsome	rs869312991
LitVar	rs869312991
Map	rs869312991
PheGenI	rs869312991
Biobank	rs869312991
1000 genomes	rs869312991
hgdp	rs869312991
ensembl	rs869312991
geneview	rs869312991
scholar	rs869312991
google	rs869312991
pharmgkb	rs869312991
gwascentral	rs869312991
openSNP	rs869312991
23andMe	rs869312991
SNPshot	rs869312991
SNPdbe	rs869312991
MSV3d	rs869312991
GWAS Ctlg	rs869312991

Max Magnitude

0

ClinVar
Risk	rs869312991(A;A)
Alt	rs869312991(A;A)
Reference	Rs869312991(C;C)
Significance	Pathogenic
Disease	Argininosuccinate lyase deficiency
Variation	info
Gene	ASL
CLNDBN	Argininosuccinate lyase deficiency
Reversed	0
HGVS	NC_000007.13:g.65553837C>A
CLNSRC
CLNACC	RCV000210606.1,