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

rs372128852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs372128852(A;A)
Make rs372128852(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position130489469
GeneASS1
is asnp
is mentioned by
dbSNPrs372128852
dbSNP (classic)rs372128852
ClinGenrs372128852
ebirs372128852
HLIrs372128852
Exacrs372128852
Gnomadrs372128852
Varsomers372128852
LitVarrs372128852
Maprs372128852
PheGenIrs372128852
Biobankrs372128852
1000 genomesrs372128852
hgdprs372128852
ensemblrs372128852
geneviewrs372128852
scholarrs372128852
googlers372128852
pharmgkbrs372128852
gwascentralrs372128852
openSNPrs372128852
23andMers372128852
23andMe allrs372128852
SNPshotrs372128852
SNPdbers372128852
MSV3drs372128852
GWAS Ctlgrs372128852
Max Magnitude0
ClinVar
Risk rs372128852(A;A)
Alt rs372128852(A;A)
Reference Rs372128852(G;G)
Significance Pathogenic
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133364856G>A
CLNSRC
CLNACC RCV000256315.1, RCV000256325.1,