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rs1064796868

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome6
Position79026002
GenePHIP
is asnp
is mentioned by
dbSNPrs1064796868
dbSNP (old)rs1064796868
ClinGenrs1064796868
ebirs1064796868
HLIrs1064796868
Exacrs1064796868
Gnomadrs1064796868
Varsomers1064796868
Maprs1064796868
PheGenIrs1064796868
Biobankrs1064796868
1000 genomesrs1064796868
hgdprs1064796868
ensemblrs1064796868
gopubmedrs1064796868
geneviewrs1064796868
scholarrs1064796868
googlers1064796868
pharmgkbrs1064796868
gwascentralrs1064796868
openSNPrs1064796868
23andMers1064796868
23andMe allrs1064796868
SNPshotrs1064796868
SNPdbers1064796868
MSV3drs1064796868
GWAS Ctlgrs1064796868
Max Magnitude0
ClinVar
Risk rs1064796868(T;T)
Alt rs1064796868(T;T)
Reference Rs1064796868(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHIP
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.79735719G>A
CLNSRC
CLNACC RCV000484481.1,