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

rs1064796911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Chromosome6
Position79015676
GenePHIP
is asnp
is mentioned by
dbSNPrs1064796911
dbSNP (old)rs1064796911
ClinGenrs1064796911
ebirs1064796911
HLIrs1064796911
Exacrs1064796911
Gnomadrs1064796911
Varsomers1064796911
LitVarrs1064796911
Maprs1064796911
PheGenIrs1064796911
Biobankrs1064796911
1000 genomesrs1064796911
hgdprs1064796911
ensemblrs1064796911
gopubmedrs1064796911
geneviewrs1064796911
scholarrs1064796911
googlers1064796911
pharmgkbrs1064796911
gwascentralrs1064796911
openSNPrs1064796911
23andMers1064796911
23andMe allrs1064796911
SNPshotrs1064796911
SNPdbers1064796911
MSV3drs1064796911
GWAS Ctlgrs1064796911
Max Magnitude0
ClinVar
Risk rs1064796911(-;-)
Alt rs1064796911(-;-)
Reference Rs1064796911(CT;CT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHIP
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.79725393_79725394delAG
CLNSRC
CLNACC RCV000483999.1,