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rs5030872

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs5030872(A;T)
Make rs5030872(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154534440
GeneG6PD
is asnp
is mentioned by
dbSNPrs5030872
ebirs5030872
HLIrs5030872
Exacrs5030872
Varsomers5030872
Maprs5030872
PheGenIrs5030872
hapmaprs5030872
1000 genomesrs5030872
hgdprs5030872
ensemblrs5030872
gopubmedrs5030872
geneviewrs5030872
scholarrs5030872
googlers5030872
pharmgkbrs5030872
gwascentralrs5030872
openSNPrs5030872
23andMers5030872
23andMe allrs5030872
SNP Nexus

SNPshotrs5030872
SNPdbers5030872
MSV3drs5030872
GWAS Ctlgrs5030872
Max Magnitude0
OMIM305900
Desc
Variant0023
Relatedalso
OMIM305900
Desc
Variant0049
Relatedalso
ClinVar
Risk rs5030872(T;T)
Alt rs5030872(T;T)
Reference rs5030872(A;A)
Significance Other
Disease G6PD SANTAMARIA G6PD MALAGA not provided Anemia
Variation info
Gene G6PD
CLNDBN G6PD SANTAMARIA G6PD MALAGA not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153762655T>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000011109.1, RCV000030892.3, RCV000079407.3, RCV000179364.1,