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rs1064796464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position91324902
GeneCCDC88C
is asnp
is mentioned by
dbSNPrs1064796464
dbSNP (old)rs1064796464
ClinGenrs1064796464
ebirs1064796464
HLIrs1064796464
Exacrs1064796464
Gnomadrs1064796464
Varsomers1064796464
Maprs1064796464
PheGenIrs1064796464
Biobankrs1064796464
1000 genomesrs1064796464
hgdprs1064796464
ensemblrs1064796464
gopubmedrs1064796464
geneviewrs1064796464
scholarrs1064796464
googlers1064796464
pharmgkbrs1064796464
gwascentralrs1064796464
openSNPrs1064796464
23andMers1064796464
23andMe allrs1064796464
SNPshotrs1064796464
SNPdbers1064796464
MSV3drs1064796464
GWAS Ctlgrs1064796464
Max Magnitude0
ClinVar
Risk rs1064796464(T;T)
Alt rs1064796464(T;T)
Reference Rs1064796464(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CCDC88C
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.91791246G>A
CLNSRC
CLNACC RCV000484539.1,