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rs1064796617

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position148828815
GeneEZH2
is asnp
is mentioned by
dbSNPrs1064796617
dbSNP (classic)rs1064796617
ClinGenrs1064796617
ebirs1064796617
HLIrs1064796617
Exacrs1064796617
Gnomadrs1064796617
Varsomers1064796617
LitVarrs1064796617
Maprs1064796617
PheGenIrs1064796617
Biobankrs1064796617
1000 genomesrs1064796617
hgdprs1064796617
ensemblrs1064796617
geneviewrs1064796617
scholarrs1064796617
googlers1064796617
pharmgkbrs1064796617
gwascentralrs1064796617
openSNPrs1064796617
23andMers1064796617
SNPshotrs1064796617
SNPdbers1064796617
MSV3drs1064796617
GWAS Ctlgrs1064796617
Max Magnitude0
ClinVar
Risk rs1064796617(C;C)
Alt rs1064796617(C;C)
Reference Rs1064796617(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EZH2
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.148525907C>G
CLNSRC
CLNACC RCV000485113.1,