Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1085307062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome3
Position134507249
GeneCEP63
is asnp
is mentioned by
dbSNPrs1085307062
dbSNP (old)rs1085307062
ClinGenrs1085307062
ebirs1085307062
HLIrs1085307062
Exacrs1085307062
Gnomadrs1085307062
Varsomers1085307062
Maprs1085307062
PheGenIrs1085307062
Biobankrs1085307062
1000 genomesrs1085307062
hgdprs1085307062
ensemblrs1085307062
gopubmedrs1085307062
geneviewrs1085307062
scholarrs1085307062
googlers1085307062
pharmgkbrs1085307062
gwascentralrs1085307062
openSNPrs1085307062
23andMers1085307062
23andMe allrs1085307062
SNPshotrs1085307062
SNPdbers1085307062
MSV3drs1085307062
GWAS Ctlgrs1085307062
Max Magnitude0
ClinVar
Risk rs1085307062(TTAA;TTAA)
Alt rs1085307062(TTAA;TTAA)
Reference Rs1085307062(-;-)
Significance Probable-Pathogenic
Disease Seckel syndrome 6
Variation info
Gene CEP63
CLNDBN Seckel syndrome 6
Reversed 0
HGVS NC_000003.11:g.134226088_134226091dupTTAA
CLNSRC
CLNACC RCV000490311.1,