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rs1057523157

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057523157(C;T)
Make rs1057523157(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position47088172
GeneSETD2
is asnp
is mentioned by
dbSNPrs1057523157
dbSNP (old)rs1057523157
ClinGenrs1057523157
ebirs1057523157
HLIrs1057523157
Exacrs1057523157
Gnomadrs1057523157
Varsomers1057523157
LitVarrs1057523157
Maprs1057523157
PheGenIrs1057523157
Biobankrs1057523157
1000 genomesrs1057523157
hgdprs1057523157
ensemblrs1057523157
gopubmedrs1057523157
geneviewrs1057523157
scholarrs1057523157
googlers1057523157
pharmgkbrs1057523157
gwascentralrs1057523157
openSNPrs1057523157
23andMers1057523157
23andMe allrs1057523157
SNPshotrs1057523157
SNPdbers1057523157
MSV3drs1057523157
GWAS Ctlgrs1057523157
Max Magnitude0
ClinVar
Risk rs1057523157(T;T)
Alt rs1057523157(T;T)
Reference Rs1057523157(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SETD2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.47129662G>A
CLNSRC
CLNACC RCV000426759.1,