Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312985

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312985(A;A)
Make rs869312985(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position66081965
GeneASL
is asnp
is mentioned by
dbSNPrs869312985
ebirs869312985
HLIrs869312985
Exacrs869312985
Varsomers869312985
Maprs869312985
PheGenIrs869312985
hapmaprs869312985
1000 genomesrs869312985
hgdprs869312985
ensemblrs869312985
gopubmedrs869312985
geneviewrs869312985
scholarrs869312985
googlers869312985
pharmgkbrs869312985
gwascentralrs869312985
openSNPrs869312985
23andMers869312985
23andMe allrs869312985
SNP Nexus

SNPshotrs869312985
SNPdbers869312985
MSV3drs869312985
GWAS Ctlgrs869312985
Max Magnitude0
ClinVar
Risk rs869312985(A;A)
Alt rs869312985(A;A)
Reference rs869312985(G;G)
Significance Pathogenic
Disease Argininosuccinate lyase deficiency
Variation info
Gene ASL
CLNDBN Argininosuccinate lyase deficiency
Reversed 0
HGVS NC_000007.13:g.65546952G>A
CLNSRC
CLNACC RCV000210603.1,