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rs78365220

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs78365220(C;C)
Make rs78365220(C;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position154535270
GeneG6PD
is asnp
is mentioned by
dbSNPrs78365220
ebirs78365220
HLIrs78365220
Exacrs78365220
Varsomers78365220
Maprs78365220
PheGenIrs78365220
hapmaprs78365220
1000 genomesrs78365220
hgdprs78365220
ensemblrs78365220
gopubmedrs78365220
geneviewrs78365220
scholarrs78365220
googlers78365220
pharmgkbrs78365220
gwascentralrs78365220
openSNPrs78365220
23andMers78365220
23andMe allrs78365220
SNP Nexus

SNPshotrs78365220
SNPdbers78365220
MSV3drs78365220
GWAS Ctlgrs78365220
Max Magnitude0
ClinVar
Risk rs78365220(C;C)
Alt rs78365220(C;C)
Reference rs78365220(T;T)
Significance Pathogenic
Disease not provided Anemia
Variation info
Gene G6PD
CLNDBN not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153763485A>G
CLNSRC HGMD
CLNACC RCV000079406.3, RCV000178824.1,