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rs1057521785

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521785(C;C)
Make rs1057521785(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position117351857
GeneCEP164
is asnp
is mentioned by
dbSNPrs1057521785
dbSNP (old)rs1057521785
ClinGenrs1057521785
ebirs1057521785
HLIrs1057521785
Exacrs1057521785
Gnomadrs1057521785
Varsomers1057521785
Maprs1057521785
PheGenIrs1057521785
Biobankrs1057521785
1000 genomesrs1057521785
hgdprs1057521785
ensemblrs1057521785
gopubmedrs1057521785
geneviewrs1057521785
scholarrs1057521785
googlers1057521785
pharmgkbrs1057521785
gwascentralrs1057521785
openSNPrs1057521785
23andMers1057521785
23andMe allrs1057521785
SNPshotrs1057521785
SNPdbers1057521785
MSV3drs1057521785
GWAS Ctlgrs1057521785
Max Magnitude0
ClinVar
Risk rs1057521785(C;C)
Alt rs1057521785(C;C)
Reference Rs1057521785(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP164
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.117222573T>C
CLNSRC
CLNACC RCV000433375.1,