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rs121908979

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908979(C;T)
Make rs121908979(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position119024957
GeneSLC37A4
is asnp
is mentioned by
dbSNPrs121908979
ebirs121908979
HLIrs121908979
Exacrs121908979
Varsomers121908979
Maprs121908979
PheGenIrs121908979
hapmaprs121908979
1000 genomesrs121908979
hgdprs121908979
ensemblrs121908979
gopubmedrs121908979
geneviewrs121908979
scholarrs121908979
googlers121908979
pharmgkbrs121908979
gwascentralrs121908979
openSNPrs121908979
23andMers121908979
23andMe allrs121908979
SNP Nexus

SNPshotrs121908979
SNPdbers121908979
MSV3drs121908979
GWAS Ctlgrs121908979
Max Magnitude0
OMIM602671
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121908979(T;T)
Alt rs121908979(T;T)
Reference rs121908979(C;C)
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.118895667G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007346.3,