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rs797044560

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044560(A;C)
Make rs797044560(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position37780111
GeneCYBB
is asnp
is mentioned by
dbSNPrs797044560
ebirs797044560
HLIrs797044560
Exacrs797044560
Varsomers797044560
Maprs797044560
PheGenIrs797044560
hapmaprs797044560
1000 genomesrs797044560
hgdprs797044560
ensemblrs797044560
gopubmedrs797044560
geneviewrs797044560
scholarrs797044560
googlers797044560
pharmgkbrs797044560
gwascentralrs797044560
openSNPrs797044560
23andMers797044560
23andMe allrs797044560
SNP Nexus

SNPshotrs797044560
SNPdbers797044560
MSV3drs797044560
GWAS Ctlgrs797044560
Max Magnitude0
ClinVar
Risk rs797044560(C;C)
Alt rs797044560(C;C)
Reference rs797044560(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CYBB
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.37639364A>C
CLNSRC
CLNACC RCV000171434.1,