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rs121908640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908640(C;T)
Make rs121908640(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130494983
GeneASS1
is asnp
is mentioned by
dbSNPrs121908640
ebirs121908640
HLIrs121908640
Exacrs121908640
Varsomers121908640
Maprs121908640
PheGenIrs121908640
hapmaprs121908640
1000 genomesrs121908640
hgdprs121908640
ensemblrs121908640
gopubmedrs121908640
geneviewrs121908640
scholarrs121908640
googlers121908640
pharmgkbrs121908640
gwascentralrs121908640
openSNPrs121908640
23andMers121908640
23andMe allrs121908640
SNP Nexus

SNPshotrs121908640
SNPdbers121908640
MSV3drs121908640
GWAS Ctlgrs121908640
Max Magnitude0
OMIM603470
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121908640(T;T)
Alt rs121908640(T;T)
Reference rs121908640(C;C)
Significance Other
Disease Citrullinemia type I not provided
Variation info
Gene ASS1
CLNDBN Citrullinemia type I not provided
Reversed 0
HGVS NC_000009.11:g.133370370C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000006700.7, RCV000185787.2,