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rs369432845

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369432845(G;T)
Make rs369432845(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position40062275
GeneBCOR
is asnp
is mentioned by
dbSNPrs369432845
dbSNP (classic)rs369432845
ClinGenrs369432845
ebirs369432845
HLIrs369432845
Exacrs369432845
Gnomadrs369432845
Varsomers369432845
LitVarrs369432845
Maprs369432845
PheGenIrs369432845
Biobankrs369432845
1000 genomesrs369432845
hgdprs369432845
ensemblrs369432845
geneviewrs369432845
scholarrs369432845
googlers369432845
pharmgkbrs369432845
gwascentralrs369432845
openSNPrs369432845
23andMers369432845
SNPshotrs369432845
SNPdbers369432845
MSV3drs369432845
GWAS Ctlgrs369432845
Max Magnitude0
ClinVar
Risk rs369432845(A;A) rs369432845(T;T)
Alt rs369432845(A;A) rs369432845(T;T)
Reference Rs369432845(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene BCOR
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000023.10:g.39921528G>T
CLNSRC
CLNACC RCV000454264.1,