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rs1064794751

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome3
Position47103416
GeneSETD2
is asnp
is mentioned by
dbSNPrs1064794751
dbSNP (old)rs1064794751
ClinGenrs1064794751
ebirs1064794751
HLIrs1064794751
Exacrs1064794751
Gnomadrs1064794751
Varsomers1064794751
Maprs1064794751
PheGenIrs1064794751
Biobankrs1064794751
1000 genomesrs1064794751
hgdprs1064794751
ensemblrs1064794751
gopubmedrs1064794751
geneviewrs1064794751
scholarrs1064794751
googlers1064794751
pharmgkbrs1064794751
gwascentralrs1064794751
openSNPrs1064794751
23andMers1064794751
23andMe allrs1064794751
SNPshotrs1064794751
SNPdbers1064794751
MSV3drs1064794751
GWAS Ctlgrs1064794751
Max Magnitude0
ClinVar
Risk rs1064794751(T;T)
Alt rs1064794751(T;T)
Reference Rs1064794751(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.47144906T>A
CLNSRC
CLNACC RCV000478163.1,