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

rs1057518579

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518579(A;C)
Make rs1057518579(C;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position37803875
GeneCYBB
is asnp
is mentioned by
dbSNPrs1057518579
dbSNP (old)rs1057518579
ClinGenrs1057518579
ebirs1057518579
HLIrs1057518579
Exacrs1057518579
Gnomadrs1057518579
Varsomers1057518579
Maprs1057518579
PheGenIrs1057518579
Biobankrs1057518579
1000 genomesrs1057518579
hgdprs1057518579
ensemblrs1057518579
gopubmedrs1057518579
geneviewrs1057518579
scholarrs1057518579
googlers1057518579
pharmgkbrs1057518579
gwascentralrs1057518579
openSNPrs1057518579
23andMers1057518579
23andMe allrs1057518579
SNPshotrs1057518579
SNPdbers1057518579
MSV3drs1057518579
GWAS Ctlgrs1057518579
Max Magnitude0
ClinVar
Risk rs1057518579(C;C)
Alt rs1057518579(C;C)
Reference Rs1057518579(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CYBB
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.37663128A>C
CLNSRC
CLNACC RCV000413530.1,