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rs1064794800

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position120538725
GeneCUL4B
is asnp
is mentioned by
dbSNPrs1064794800
dbSNP (old)rs1064794800
ClinGenrs1064794800
ebirs1064794800
HLIrs1064794800
Exacrs1064794800
Gnomadrs1064794800
Varsomers1064794800
Maprs1064794800
PheGenIrs1064794800
Biobankrs1064794800
1000 genomesrs1064794800
hgdprs1064794800
ensemblrs1064794800
gopubmedrs1064794800
geneviewrs1064794800
scholarrs1064794800
googlers1064794800
pharmgkbrs1064794800
gwascentralrs1064794800
openSNPrs1064794800
23andMers1064794800
23andMe allrs1064794800
SNPshotrs1064794800
SNPdbers1064794800
MSV3drs1064794800
GWAS Ctlgrs1064794800
Max Magnitude0
ClinVar
Risk rs1064794800(T;T)
Alt rs1064794800(T;T)
Reference Rs1064794800(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CUL4B
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.119672580C>A
CLNSRC
CLNACC RCV000479459.1,