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rs1064793152

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
ChromosomeX
Position53320828
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs1064793152
dbSNP (old)rs1064793152
ClinGenrs1064793152
ebirs1064793152
HLIrs1064793152
Exacrs1064793152
Gnomadrs1064793152
Varsomers1064793152
Maprs1064793152
PheGenIrs1064793152
Biobankrs1064793152
1000 genomesrs1064793152
hgdprs1064793152
ensemblrs1064793152
gopubmedrs1064793152
geneviewrs1064793152
scholarrs1064793152
googlers1064793152
pharmgkbrs1064793152
gwascentralrs1064793152
openSNPrs1064793152
23andMers1064793152
23andMe allrs1064793152
SNPshotrs1064793152
SNPdbers1064793152
MSV3drs1064793152
GWAS Ctlgrs1064793152
Max Magnitude0
ClinVar
Risk rs1064793152(-;-)
Alt rs1064793152(-;-)
Reference Rs1064793152(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene IQSEC2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53350026delT
CLNSRC
CLNACC RCV000485376.1,