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rs121908643

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908643(C;T)
Make rs121908643(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130452281
GeneASS1
is asnp
is mentioned by
dbSNPrs121908643
ebirs121908643
HLIrs121908643
Exacrs121908643
Varsomers121908643
Maprs121908643
PheGenIrs121908643
hapmaprs121908643
1000 genomesrs121908643
hgdprs121908643
ensemblrs121908643
gopubmedrs121908643
geneviewrs121908643
scholarrs121908643
googlers121908643
pharmgkbrs121908643
gwascentralrs121908643
openSNPrs121908643
23andMers121908643
23andMe allrs121908643
SNP Nexus

SNPshotrs121908643
SNPdbers121908643
MSV3drs121908643
GWAS Ctlgrs121908643
Max Magnitude0
OMIM603470
Desc
Variant0011
Relatedalso
ClinVar
Risk rs121908643(T;T)
Alt rs121908643(T;T)
Reference rs121908643(C;C)
Significance Pathogenic
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133327668C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006703.3,