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rs797044924

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044924(A;G)
Make rs797044924(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position15331833
GenePIGA
is asnp
is mentioned by
dbSNPrs797044924
ebirs797044924
HLIrs797044924
Exacrs797044924
Varsomers797044924
Maprs797044924
PheGenIrs797044924
hapmaprs797044924
1000 genomesrs797044924
hgdprs797044924
ensemblrs797044924
gopubmedrs797044924
geneviewrs797044924
scholarrs797044924
googlers797044924
pharmgkbrs797044924
gwascentralrs797044924
openSNPrs797044924
23andMers797044924
23andMe allrs797044924
SNP Nexus

SNPshotrs797044924
SNPdbers797044924
MSV3drs797044924
GWAS Ctlgrs797044924
Max Magnitude0
ClinVar
Risk rs797044924(G;G)
Alt rs797044924(G;G)
Reference rs797044924(A;A)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PIGA
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.15349955T>C
CLNSRC
CLNACC RCV000190762.1,