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rs121908975

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908975(G;T)
Make rs121908975(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119025251
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs121908975
ebirs121908975
HLIrs121908975
Exacrs121908975
Varsomers121908975
Maprs121908975
PheGenIrs121908975
hapmaprs121908975
1000 genomesrs121908975
hgdprs121908975
ensemblrs121908975
gopubmedrs121908975
geneviewrs121908975
scholarrs121908975
googlers121908975
pharmgkbrs121908975
gwascentralrs121908975
openSNPrs121908975
23andMers121908975
23andMe allrs121908975
SNP Nexus

SNPshotrs121908975
SNPdbers121908975
MSV3drs121908975
GWAS Ctlgrs121908975
Max Magnitude0
OMIM602671
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908975(A,T;A,T)
Alt rs121908975(A,T;A,T)
Reference rs121908975(G;G)
Significance Pathogenic
Disease Glucose-6-phosphate transport defect
Variation info
Gene SLC37A4
CLNDBN Glucose-6-phosphate transport defect
Reversed 1
HGVS NC_000011.9:g.118895961C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007331.3,