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rs121909307

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909307(A;A)
Make rs121909307(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position34942488
GeneGSS
is asnp
is mentioned by
dbSNPrs121909307
ebirs121909307
HLIrs121909307
Exacrs121909307
Varsomers121909307
Maprs121909307
PheGenIrs121909307
hapmaprs121909307
1000 genomesrs121909307
hgdprs121909307
ensemblrs121909307
gopubmedrs121909307
geneviewrs121909307
scholarrs121909307
googlers121909307
pharmgkbrs121909307
gwascentralrs121909307
openSNPrs121909307
23andMers121909307
23andMe allrs121909307
SNP Nexus

SNPshotrs121909307
SNPdbers121909307
MSV3drs121909307
GWAS Ctlgrs121909307
Max Magnitude0
OMIM601002
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909307(A;A)
Alt rs121909307(A;A)
Reference rs121909307(G;G)
Significance Pathogenic
Disease Gluthathione synthetase deficiency
Variation info
Gene GSS
CLNDBN Gluthathione synthetase deficiency
Reversed 1
HGVS NC_000020.10:g.33530291C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009051.3,