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

rs1057524571

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524571(G;G)
Make rs1057524571(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position64807550
GeneMEN1
is asnp
is mentioned by
dbSNPrs1057524571
dbSNP (old)rs1057524571
ClinGenrs1057524571
ebirs1057524571
HLIrs1057524571
Exacrs1057524571
Gnomadrs1057524571
Varsomers1057524571
Maprs1057524571
PheGenIrs1057524571
Biobankrs1057524571
1000 genomesrs1057524571
hgdprs1057524571
ensemblrs1057524571
gopubmedrs1057524571
geneviewrs1057524571
scholarrs1057524571
googlers1057524571
pharmgkbrs1057524571
gwascentralrs1057524571
openSNPrs1057524571
23andMers1057524571
23andMe allrs1057524571
SNPshotrs1057524571
SNPdbers1057524571
MSV3drs1057524571
GWAS Ctlgrs1057524571
Max Magnitude0
ClinVar
Risk rs1057524571(G;G)
Alt rs1057524571(G;G)
Reference Rs1057524571(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575022A>C
CLNSRC
CLNACC RCV000430267.1,