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rs398124313

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398124313(-;-)
Make rs398124313(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position40064370
GeneBCOR
is asnp
is mentioned by
dbSNPrs398124313
ebirs398124313
HLIrs398124313
Exacrs398124313
Varsomers398124313
Maprs398124313
PheGenIrs398124313
hapmaprs398124313
1000 genomesrs398124313
hgdprs398124313
ensemblrs398124313
gopubmedrs398124313
geneviewrs398124313
scholarrs398124313
googlers398124313
pharmgkbrs398124313
gwascentralrs398124313
openSNPrs398124313
23andMers398124313
23andMe allrs398124313
SNP Nexus

SNPshotrs398124313
SNPdbers398124313
MSV3drs398124313
GWAS Ctlgrs398124313
Max Magnitude0
ClinVar
Risk rs398124313(;)
Alt rs398124313(;)
Reference rs398124313(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene BCOR
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.39923623delA
CLNSRC ClinVar
CLNACC RCV000081815.4,