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rs137852319

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852319(G;G)
Make rs137852319(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154534157
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852319
ebirs137852319
HLIrs137852319
Exacrs137852319
Varsomers137852319
Maprs137852319
PheGenIrs137852319
hapmaprs137852319
1000 genomesrs137852319
hgdprs137852319
ensemblrs137852319
gopubmedrs137852319
geneviewrs137852319
scholarrs137852319
googlers137852319
pharmgkbrs137852319
gwascentralrs137852319
openSNPrs137852319
23andMers137852319
23andMe allrs137852319
SNP Nexus

SNPshotrs137852319
SNPdbers137852319
MSV3drs137852319
GWAS Ctlgrs137852319
Max Magnitude0
OMIM305900
Desc
Variant0011
Relatedalso
ClinVar
Risk rs137852319(G;G)
Alt rs137852319(G;G)
Reference rs137852319(T;T)
Significance Other
Disease G6PD HARILAOU
Variation info
Gene G6PD
CLNDBN G6PD HARILAOU
Reversed 1
HGVS NC_000023.10:g.153762372A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000011094.1,