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rs137852329

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852329(A;A)
Make rs137852329(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154532765
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852329
ebirs137852329
HLIrs137852329
Exacrs137852329
Varsomers137852329
Maprs137852329
PheGenIrs137852329
hapmaprs137852329
1000 genomesrs137852329
hgdprs137852329
ensemblrs137852329
gopubmedrs137852329
geneviewrs137852329
scholarrs137852329
googlers137852329
pharmgkbrs137852329
gwascentralrs137852329
openSNPrs137852329
23andMers137852329
23andMe allrs137852329
SNP Nexus

SNPshotrs137852329
SNPdbers137852329
MSV3drs137852329
GWAS Ctlgrs137852329
Max Magnitude0
OMIM305900
Desc
Variant0030
Relatedalso
ClinVar
Risk rs137852329(A;A)
Alt rs137852329(A;A)
Reference rs137852329(C;C)
Significance Other
Disease G6PD LOMA LINDA Anemia
Variation info
Gene G6PD
CLNDBN G6PD LOMA LINDA Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153760980G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011125.3, RCV000066262.4,