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rs121908641

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908641(A;A)
Make rs121908641(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130499545
GeneASS1
is asnp
is mentioned by
dbSNPrs121908641
ebirs121908641
HLIrs121908641
Exacrs121908641
Varsomers121908641
Maprs121908641
PheGenIrs121908641
hapmaprs121908641
1000 genomesrs121908641
hgdprs121908641
ensemblrs121908641
gopubmedrs121908641
geneviewrs121908641
scholarrs121908641
googlers121908641
pharmgkbrs121908641
gwascentralrs121908641
openSNPrs121908641
23andMers121908641
23andMe allrs121908641
SNP Nexus

SNPshotrs121908641
SNPdbers121908641
MSV3drs121908641
GWAS Ctlgrs121908641
Max Magnitude0
OMIM603470
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908641(A,T;A,T)
Alt rs121908641(A,T;A,T)
Reference rs121908641(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.133374932G>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000006701.5, RCV000185789.2,