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rs121908645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908645(C;T)
Make rs121908645(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position130480446
GeneASS1
is asnp
is mentioned by
dbSNPrs121908645
ebirs121908645
HLIrs121908645
Exacrs121908645
Varsomers121908645
Maprs121908645
PheGenIrs121908645
hapmaprs121908645
1000 genomesrs121908645
hgdprs121908645
ensemblrs121908645
gopubmedrs121908645
geneviewrs121908645
scholarrs121908645
googlers121908645
pharmgkbrs121908645
gwascentralrs121908645
openSNPrs121908645
23andMers121908645
23andMe allrs121908645
SNP Nexus

SNPshotrs121908645
SNPdbers121908645
MSV3drs121908645
GWAS Ctlgrs121908645
Max Magnitude0
OMIM603470
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121908645(T;T)
Alt rs121908645(T;T)
Reference rs121908645(C;C)
Significance Other
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133355833C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006705.5,