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rs121908639

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908639(A;A)
Make rs121908639(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position130489464
GeneASS1
is asnp
is mentioned by
dbSNPrs121908639
ebirs121908639
HLIrs121908639
Exacrs121908639
Varsomers121908639
Maprs121908639
PheGenIrs121908639
hapmaprs121908639
1000 genomesrs121908639
hgdprs121908639
ensemblrs121908639
gopubmedrs121908639
geneviewrs121908639
scholarrs121908639
googlers121908639
pharmgkbrs121908639
gwascentralrs121908639
openSNPrs121908639
23andMers121908639
23andMe allrs121908639
SNP Nexus

SNPshotrs121908639
SNPdbers121908639
MSV3drs121908639
GWAS Ctlgrs121908639
Max Magnitude0
OMIM603470
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908639(A;A)
Alt rs121908639(A;A)
Reference rs121908639(G;G)
Significance Other
Disease Citrullinemia type I
Variation info
Gene ASS1
CLNDBN Citrullinemia type I
Reversed 0
HGVS NC_000009.11:g.133364851G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006699.4,