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rs727503826

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503826(A;A)
Make rs727503826(A;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position40074570
GeneBCOR
is asnp
is mentioned by
dbSNPrs727503826
ebirs727503826
HLIrs727503826
Exacrs727503826
Varsomers727503826
Maprs727503826
PheGenIrs727503826
hapmaprs727503826
1000 genomesrs727503826
hgdprs727503826
ensemblrs727503826
gopubmedrs727503826
geneviewrs727503826
scholarrs727503826
googlers727503826
pharmgkbrs727503826
gwascentralrs727503826
openSNPrs727503826
23andMers727503826
23andMe allrs727503826
SNP Nexus

SNPshotrs727503826
SNPdbers727503826
MSV3drs727503826
GWAS Ctlgrs727503826
Max Magnitude0
ClinVar
Risk rs727503826(A;A)
Alt rs727503826(A;A)
Reference rs727503826(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene BCOR
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.39933823G>T
CLNSRC
CLNACC RCV000152859.3,