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rs121908648

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908648(A;C)
Make rs121908648(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position130489422
GeneASS1
is asnp
is mentioned by
dbSNPrs121908648
ebirs121908648
HLIrs121908648
Exacrs121908648
Varsomers121908648
Maprs121908648
PheGenIrs121908648
hapmaprs121908648
1000 genomesrs121908648
hgdprs121908648
ensemblrs121908648
gopubmedrs121908648
geneviewrs121908648
scholarrs121908648
googlers121908648
pharmgkbrs121908648
gwascentralrs121908648
openSNPrs121908648
23andMers121908648
23andMe allrs121908648
SNP Nexus

SNPshotrs121908648
SNPdbers121908648
MSV3drs121908648
GWAS Ctlgrs121908648
Max Magnitude0
OMIM603470
Desc
Variant0019
Relatedalso
ClinVar
Risk rs121908648(C;C)
Alt rs121908648(C;C)
Reference rs121908648(A;A)
Significance Pathogenic
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133364809A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006711.3,