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rs1064793475

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
ChromosomeX
Position30308618
GeneNR0B1
is asnp
is mentioned by
dbSNPrs1064793475
dbSNP (old)rs1064793475
ClinGenrs1064793475
ebirs1064793475
HLIrs1064793475
Exacrs1064793475
Gnomadrs1064793475
Varsomers1064793475
Maprs1064793475
PheGenIrs1064793475
Biobankrs1064793475
1000 genomesrs1064793475
hgdprs1064793475
ensemblrs1064793475
gopubmedrs1064793475
geneviewrs1064793475
scholarrs1064793475
googlers1064793475
pharmgkbrs1064793475
gwascentralrs1064793475
openSNPrs1064793475
23andMers1064793475
23andMe allrs1064793475
SNPshotrs1064793475
SNPdbers1064793475
MSV3drs1064793475
GWAS Ctlgrs1064793475
Max Magnitude0
ClinVar
Risk rs1064793475(-;-)
Alt rs1064793475(-;-)
Reference Rs1064793475(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene NR0B1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.30326735_30326736delTT
CLNSRC
CLNACC RCV000479228.1,