Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057521937

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057521937(A;T)
Make rs1057521937(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position37805085
GeneCYBB
is asnp
is mentioned by
dbSNPrs1057521937
dbSNP (old)rs1057521937
ClinGenrs1057521937
ebirs1057521937
HLIrs1057521937
Exacrs1057521937
Gnomadrs1057521937
Varsomers1057521937
Maprs1057521937
PheGenIrs1057521937
Biobankrs1057521937
1000 genomesrs1057521937
hgdprs1057521937
ensemblrs1057521937
gopubmedrs1057521937
geneviewrs1057521937
scholarrs1057521937
googlers1057521937
pharmgkbrs1057521937
gwascentralrs1057521937
openSNPrs1057521937
23andMers1057521937
23andMe allrs1057521937
SNPshotrs1057521937
SNPdbers1057521937
MSV3drs1057521937
GWAS Ctlgrs1057521937
Max Magnitude0
ClinVar
Risk rs1057521937(T;T)
Alt rs1057521937(T;T)
Reference Rs1057521937(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYBB
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.37664338A>T
CLNSRC
CLNACC RCV000424658.1,