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rs1057517778

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517778(-;-)
Make rs1057517778(-;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position30308784
GeneNR0B1
is asnp
is mentioned by
dbSNPrs1057517778
dbSNP (old)rs1057517778
ClinGenrs1057517778
ebirs1057517778
HLIrs1057517778
Exacrs1057517778
Gnomadrs1057517778
Varsomers1057517778
Maprs1057517778
PheGenIrs1057517778
Biobankrs1057517778
1000 genomesrs1057517778
hgdprs1057517778
ensemblrs1057517778
gopubmedrs1057517778
geneviewrs1057517778
scholarrs1057517778
googlers1057517778
pharmgkbrs1057517778
gwascentralrs1057517778
openSNPrs1057517778
23andMers1057517778
23andMe allrs1057517778
SNPshotrs1057517778
SNPdbers1057517778
MSV3drs1057517778
GWAS Ctlgrs1057517778
Max Magnitude0
ClinVar
Risk rs1057517778(-;-)
Alt rs1057517778(-;-)
Reference Rs1057517778(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NR0B1
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.30326901delC
CLNSRC
CLNACC RCV000413027.1,