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

rs869312990

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312990(A;A)
Make rs869312990(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position66087796
GeneASL
is asnp
is mentioned by
dbSNPrs869312990
ebirs869312990
HLIrs869312990
Exacrs869312990
Varsomers869312990
Maprs869312990
PheGenIrs869312990
hapmaprs869312990
1000 genomesrs869312990
hgdprs869312990
ensemblrs869312990
gopubmedrs869312990
geneviewrs869312990
scholarrs869312990
googlers869312990
pharmgkbrs869312990
gwascentralrs869312990
openSNPrs869312990
23andMers869312990
23andMe allrs869312990
SNP Nexus

SNPshotrs869312990
SNPdbers869312990
MSV3drs869312990
GWAS Ctlgrs869312990
Max Magnitude0
ClinVar
Risk rs869312990(A;A)
Alt rs869312990(A;A)
Reference rs869312990(G;G)
Significance Pathogenic
Disease Argininosuccinate lyase deficiency
Variation info
Gene ASL
CLNDBN Argininosuccinate lyase deficiency
Reversed 0
HGVS NC_000007.13:g.65552783G>A
CLNSRC
CLNACC RCV000210713.1,