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rs886041215

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
ChromosomeX
Position30304691
GeneNR0B1
is asnp
is mentioned by
dbSNPrs886041215
dbSNP (classic)rs886041215
ClinGenrs886041215
ebirs886041215
HLIrs886041215
Exacrs886041215
Gnomadrs886041215
Varsomers886041215
LitVarrs886041215
Maprs886041215
PheGenIrs886041215
Biobankrs886041215
1000 genomesrs886041215
hgdprs886041215
ensemblrs886041215
geneviewrs886041215
scholarrs886041215
googlers886041215
pharmgkbrs886041215
gwascentralrs886041215
openSNPrs886041215
23andMers886041215
23andMe allrs886041215
SNPshotrs886041215
SNPdbers886041215
MSV3drs886041215
GWAS Ctlgrs886041215
Max Magnitude0
ClinVar
Risk rs886041215(-;-)
Alt rs886041215(-;-)
Reference Rs886041215(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NR0B1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.30322808delA
CLNSRC
CLNACC RCV000260370.1,