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rs151344482

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151344482(A;G)
Make rs151344482(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position37796093
GeneCYBB
is asnp
is mentioned by
dbSNPrs151344482
dbSNP (classic)rs151344482
ClinGenrs151344482
ebirs151344482
HLIrs151344482
Exacrs151344482
Gnomadrs151344482
Varsomers151344482
LitVarrs151344482
Maprs151344482
PheGenIrs151344482
Biobankrs151344482
1000 genomesrs151344482
hgdprs151344482
ensemblrs151344482
geneviewrs151344482
scholarrs151344482
googlers151344482
pharmgkbrs151344482
gwascentralrs151344482
openSNPrs151344482
23andMers151344482
23andMe allrs151344482
SNPshotrs151344482
SNPdbers151344482
MSV3drs151344482
GWAS Ctlgrs151344482
Max Magnitude0
ClinVar
Risk rs151344482(G;G)
Alt rs151344482(G;G)
Reference Rs151344482(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYBB
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.37655346A>G
CLNSRC UniProtKB (protein) UniProtKB (variants)
CLNACC RCV000059266.1,