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

rs398123131

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123131(A;A)
Make rs398123131(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130480405
GeneASS1
is asnp
is mentioned by
dbSNPrs398123131
ebirs398123131
HLIrs398123131
Exacrs398123131
Varsomers398123131
Maprs398123131
PheGenIrs398123131
hapmaprs398123131
1000 genomesrs398123131
hgdprs398123131
ensemblrs398123131
gopubmedrs398123131
geneviewrs398123131
scholarrs398123131
googlers398123131
pharmgkbrs398123131
gwascentralrs398123131
openSNPrs398123131
23andMers398123131
23andMe allrs398123131
SNP Nexus

SNPshotrs398123131
SNPdbers398123131
MSV3drs398123131
GWAS Ctlgrs398123131
Max Magnitude0
ClinVar
Risk rs398123131(A;A)
Alt rs398123131(A;A)
Reference rs398123131(G;G)
Significance Pathogenic
Disease Citrullinemia type I not provided
Variation info
Gene ASS1
CLNDBN Citrullinemia type I not provided
Reversed 0
HGVS NC_000009.11:g.133355792G>A
CLNSRC HGMD
CLNACC RCV000078026.4, RCV000185784.1,