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rs121909308

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909308(C;T)
Make rs121909308(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position34935611
GeneGSS
is asnp
is mentioned by
dbSNPrs121909308
ebirs121909308
HLIrs121909308
Exacrs121909308
Varsomers121909308
Maprs121909308
PheGenIrs121909308
hapmaprs121909308
1000 genomesrs121909308
hgdprs121909308
ensemblrs121909308
gopubmedrs121909308
geneviewrs121909308
scholarrs121909308
googlers121909308
pharmgkbrs121909308
gwascentralrs121909308
openSNPrs121909308
23andMers121909308
23andMe allrs121909308
SNP Nexus

SNPshotrs121909308
SNPdbers121909308
MSV3drs121909308
GWAS Ctlgrs121909308
Max Magnitude0
OMIM601002
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121909308(T;T)
Alt rs121909308(T;T)
Reference rs121909308(C;C)
Significance Pathogenic
Disease Gluthathione synthetase deficiency
Variation info
Gene GSS
CLNDBN Gluthathione synthetase deficiency
Reversed 1
HGVS NC_000020.10:g.33523414G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009053.3,