Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057520733

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520733(C;T)
Make rs1057520733(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807554
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057520733
dbSNP (old)rs1057520733
ClinGenrs1057520733
ebirs1057520733
HLIrs1057520733
Exacrs1057520733
Gnomadrs1057520733
Varsomers1057520733
LitVarrs1057520733
Maprs1057520733
PheGenIrs1057520733
Biobankrs1057520733
1000 genomesrs1057520733
hgdprs1057520733
ensemblrs1057520733
gopubmedrs1057520733
geneviewrs1057520733
scholarrs1057520733
googlers1057520733
pharmgkbrs1057520733
gwascentralrs1057520733
openSNPrs1057520733
23andMers1057520733
23andMe allrs1057520733
SNPshotrs1057520733
SNPdbers1057520733
MSV3drs1057520733
GWAS Ctlgrs1057520733
Max Magnitude0
ClinVar
Risk rs1057520733(T;T)
Alt rs1057520733(T;T)
Reference Rs1057520733(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575026G>A
CLNSRC
CLNACC RCV000419478.1,