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rs137852338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TCA;TCA) 0 common in clinvar
Make rs137852338(-;-)
Make rs137852338(-;ATC)
Make rs137852338(ATC;ATC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154546051
GeneG6PD, IKBKG
is asnp
is mentioned by
dbSNPrs137852338
ebirs137852338
HLIrs137852338
Exacrs137852338
Varsomers137852338
Maprs137852338
PheGenIrs137852338
hapmaprs137852338
1000 genomesrs137852338
hgdprs137852338
ensemblrs137852338
gopubmedrs137852338
geneviewrs137852338
scholarrs137852338
googlers137852338
pharmgkbrs137852338
gwascentralrs137852338
openSNPrs137852338
23andMers137852338
23andMe allrs137852338
SNP Nexus

SNPshotrs137852338
SNPdbers137852338
MSV3drs137852338
GWAS Ctlgrs137852338
Max Magnitude0
OMIM305900
Desc
Variant0041
Relatedalso
ClinVar
Risk rs137852338(;)
Alt rs137852338(;)
Reference rs137852338(CAT;CAT)
Significance Other
Disease G6PD SUNDERLAND Anemia
Variation info
Gene IKBKG G6PD
CLNDBN G6PD SUNDERLAND Anemia, nonspherocytic hemolytic, due to G6PD deficiency
Reversed 1
HGVS NC_000023.10:g.153774266_153774268delGAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000011140.2, RCV000011141.3,