rs869312985

Orientation

plus

Stabilized

plus

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

Make rs869312985(A;A)

Make rs869312985(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

66081965

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs869312985
dbSNP (classic)	rs869312985
ClinGen	rs869312985
ebi	rs869312985
HLI	rs869312985
Exac	rs869312985
Gnomad	rs869312985
Varsome	rs869312985
LitVar	rs869312985
Map	rs869312985
PheGenI	rs869312985
Biobank	rs869312985
1000 genomes	rs869312985
hgdp	rs869312985
ensembl	rs869312985
geneview	rs869312985
scholar	rs869312985
google	rs869312985
pharmgkb	rs869312985
gwascentral	rs869312985
openSNP	rs869312985
23andMe	rs869312985
SNPshot	rs869312985
SNPdbe	rs869312985
MSV3d	rs869312985
GWAS Ctlg	rs869312985

Max Magnitude

0

ClinVar
Risk	rs869312985(A;A)
Alt	rs869312985(A;A)
Reference	Rs869312985(G;G)
Significance	Pathogenic
Disease	Argininosuccinate lyase deficiency not provided
Variation	info
Gene	ASL
CLNDBN	Argininosuccinate lyase deficiency not provided
Reversed	0
HGVS	NC_000007.13:g.65546952G>A
CLNSRC
CLNACC	RCV000210603.1, RCV000489282.1,