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rs1064795661

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome3
Position47017255
GeneSETD2
is asnp
is mentioned by
dbSNPrs1064795661
dbSNP (old)rs1064795661
ClinGenrs1064795661
ebirs1064795661
HLIrs1064795661
Exacrs1064795661
Gnomadrs1064795661
Varsomers1064795661
LitVarrs1064795661
Maprs1064795661
PheGenIrs1064795661
Biobankrs1064795661
1000 genomesrs1064795661
hgdprs1064795661
ensemblrs1064795661
gopubmedrs1064795661
geneviewrs1064795661
scholarrs1064795661
googlers1064795661
pharmgkbrs1064795661
gwascentralrs1064795661
openSNPrs1064795661
23andMers1064795661
23andMe allrs1064795661
SNPshotrs1064795661
SNPdbers1064795661
MSV3drs1064795661
GWAS Ctlgrs1064795661
Max Magnitude0
ClinVar
Risk rs1064795661(T;T)
Alt rs1064795661(T;T)
Reference Rs1064795661(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SETD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.47058745C>A
CLNSRC
CLNACC RCV000483102.1,