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rs72554664

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554664(A;A)
Make rs72554664(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154532257
GeneG6PD
is asnp
is mentioned by
dbSNPrs72554664
ebirs72554664
HLIrs72554664
Exacrs72554664
Varsomers72554664
Maprs72554664
PheGenIrs72554664
hapmaprs72554664
1000 genomesrs72554664
hgdprs72554664
ensemblrs72554664
gopubmedrs72554664
geneviewrs72554664
scholarrs72554664
googlers72554664
pharmgkbrs72554664
gwascentralrs72554664
openSNPrs72554664
23andMers72554664
23andMe allrs72554664
SNP Nexus

SNPshotrs72554664
SNPdbers72554664
MSV3drs72554664
GWAS Ctlgrs72554664
Max Magnitude0
OMIM305900
Desc
Variant0029
Relatedalso


ClinVar
Risk rs72554664(A;A)
Alt rs72554664(A;A)
Reference rs72554664(G;G)
Significance Other
Disease G6PD KAIPING G6PD ANANT G6PD DHON G6PD PETRICH-LIKE G6PD SAPPORO-LIKE not provided Anemia
Variation info
Gene G6PD
CLNDBN G6PD KAIPING G6PD ANANT G6PD DHON G6PD PETRICH-LIKE G6PD SAPPORO-LIKE not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153760472C>T
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000011120.2, RCV000011121.2, RCV000011122.2, RCV000011123.2, RCV000011124.2, RCV000079399.3, RCV000174271.1,