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rs1064794733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position53199082
GeneKDM5C, MIR6894
is asnp
is mentioned by
dbSNPrs1064794733
dbSNP (old)rs1064794733
ClinGenrs1064794733
ebirs1064794733
HLIrs1064794733
Exacrs1064794733
Gnomadrs1064794733
Varsomers1064794733
LitVarrs1064794733
Maprs1064794733
PheGenIrs1064794733
Biobankrs1064794733
1000 genomesrs1064794733
hgdprs1064794733
ensemblrs1064794733
gopubmedrs1064794733
geneviewrs1064794733
scholarrs1064794733
googlers1064794733
pharmgkbrs1064794733
gwascentralrs1064794733
openSNPrs1064794733
23andMers1064794733
23andMe allrs1064794733
SNPshotrs1064794733
SNPdbers1064794733
MSV3drs1064794733
GWAS Ctlgrs1064794733
Max Magnitude0
ClinVar
Risk rs1064794733(T;T)
Alt rs1064794733(T;T)
Reference Rs1064794733(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6894 KDM5C
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53228264G>A
CLNSRC
CLNACC RCV000480561.1,