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rs121908638

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908638(A;A)
Make rs121908638(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130470877
GeneASS1
is asnp
is mentioned by
dbSNPrs121908638
ebirs121908638
HLIrs121908638
Exacrs121908638
Varsomers121908638
Maprs121908638
PheGenIrs121908638
hapmaprs121908638
1000 genomesrs121908638
hgdprs121908638
ensemblrs121908638
gopubmedrs121908638
geneviewrs121908638
scholarrs121908638
googlers121908638
pharmgkbrs121908638
gwascentralrs121908638
openSNPrs121908638
23andMers121908638
23andMe allrs121908638
SNP Nexus

SNPshotrs121908638
SNPdbers121908638
MSV3drs121908638
GWAS Ctlgrs121908638
Max Magnitude0
OMIM603470
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908638(A;A)
Alt rs121908638(A;A)
Reference rs121908638(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.133346264G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006698.2, RCV000185782.2,