Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064796062

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome16
Position67629510
GeneCTCF
is asnp
is mentioned by
dbSNPrs1064796062
dbSNP (classic)rs1064796062
ClinGenrs1064796062
ebirs1064796062
HLIrs1064796062
Exacrs1064796062
Gnomadrs1064796062
Varsomers1064796062
LitVarrs1064796062
Maprs1064796062
PheGenIrs1064796062
Biobankrs1064796062
1000 genomesrs1064796062
hgdprs1064796062
ensemblrs1064796062
geneviewrs1064796062
scholarrs1064796062
googlers1064796062
pharmgkbrs1064796062
gwascentralrs1064796062
openSNPrs1064796062
23andMers1064796062
23andMe allrs1064796062
SNPshotrs1064796062
SNPdbers1064796062
MSV3drs1064796062
GWAS Ctlgrs1064796062
Max Magnitude0
ClinVar
Risk rs1064796062(-;-)
Alt rs1064796062(-;-)
Reference Rs1064796062(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CTCF
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.67663413delA
CLNSRC
CLNACC RCV000485210.1,