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rs1064795080

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position88429143
GeneZNF469
is asnp
is mentioned by
dbSNPrs1064795080
dbSNP (old)rs1064795080
ClinGenrs1064795080
ebirs1064795080
HLIrs1064795080
Exacrs1064795080
Gnomadrs1064795080
Varsomers1064795080
LitVarrs1064795080
Maprs1064795080
PheGenIrs1064795080
Biobankrs1064795080
1000 genomesrs1064795080
hgdprs1064795080
ensemblrs1064795080
gopubmedrs1064795080
geneviewrs1064795080
scholarrs1064795080
googlers1064795080
pharmgkbrs1064795080
gwascentralrs1064795080
openSNPrs1064795080
23andMers1064795080
23andMe allrs1064795080
SNPshotrs1064795080
SNPdbers1064795080
MSV3drs1064795080
GWAS Ctlgrs1064795080
Max Magnitude0
ClinVar
Risk rs1064795080(-;-)
Alt rs1064795080(-;-)
Reference Rs1064795080(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZNF469
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.88495551delC
CLNSRC
CLNACC RCV000480677.1,