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rs1057517730

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGAG;TGAG) 0 common in clinvar
Make rs1057517730(-;-)
Make rs1057517730(-;AGTG)
Make rs1057517730(AGTG;AGTG)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position37796145
GeneCYBB
is asnp
is mentioned by
dbSNPrs1057517730
dbSNP (old)rs1057517730
ClinGenrs1057517730
ebirs1057517730
HLIrs1057517730
Exacrs1057517730
Gnomadrs1057517730
Varsomers1057517730
LitVarrs1057517730
Maprs1057517730
PheGenIrs1057517730
Biobankrs1057517730
1000 genomesrs1057517730
hgdprs1057517730
ensemblrs1057517730
gopubmedrs1057517730
geneviewrs1057517730
scholarrs1057517730
googlers1057517730
pharmgkbrs1057517730
gwascentralrs1057517730
openSNPrs1057517730
23andMers1057517730
23andMe allrs1057517730
SNPshotrs1057517730
SNPdbers1057517730
MSV3drs1057517730
GWAS Ctlgrs1057517730
Max Magnitude0
ClinVar
Risk rs1057517730(-;-)
Alt rs1057517730(-;-)
Reference Rs1057517730(TGAG;TGAG)
Significance Pathogenic
Disease not provided
Variation info
Gene CYBB
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.37655398_37655401delAGTG
CLNSRC
CLNACC RCV000412938.1,