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rs137852315

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852315(A;A)
Make rs137852315(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154536032
GeneG6PD
is asnp
is mentioned by
dbSNPrs137852315
ebirs137852315
HLIrs137852315
Exacrs137852315
Varsomers137852315
Maprs137852315
PheGenIrs137852315
hapmaprs137852315
1000 genomesrs137852315
hgdprs137852315
ensemblrs137852315
gopubmedrs137852315
geneviewrs137852315
scholarrs137852315
googlers137852315
pharmgkbrs137852315
gwascentralrs137852315
openSNPrs137852315
23andMers137852315
23andMe allrs137852315
SNP Nexus

SNPshotrs137852315
SNPdbers137852315
MSV3drs137852315
GWAS Ctlgrs137852315
Max Magnitude0
OMIM305900
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852315(A;A)
Alt rs137852315(A;A)
Reference rs137852315(G;G)
Significance Other
Disease G6PD METAPONTO
Variation info
Gene G6PD
CLNDBN G6PD METAPONTO
Reversed 1
HGVS NC_000023.10:g.153764247C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011089.2,