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

rs1060500759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060500759(C;T)
Make rs1060500759(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position43120162
GeneRET
is asnp
is mentioned by
dbSNPrs1060500759
dbSNP (old)rs1060500759
ClinGenrs1060500759
ebirs1060500759
HLIrs1060500759
Exacrs1060500759
Gnomadrs1060500759
Varsomers1060500759
Maprs1060500759
PheGenIrs1060500759
Biobankrs1060500759
1000 genomesrs1060500759
hgdprs1060500759
ensemblrs1060500759
gopubmedrs1060500759
geneviewrs1060500759
scholarrs1060500759
googlers1060500759
pharmgkbrs1060500759
gwascentralrs1060500759
openSNPrs1060500759
23andMers1060500759
23andMe allrs1060500759
SNPshotrs1060500759
SNPdbers1060500759
MSV3drs1060500759
GWAS Ctlgrs1060500759
Max Magnitude0
ClinVar
Risk rs1060500759(T;T)
Alt rs1060500759(T;T)
Reference Rs1060500759(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2
Reversed 0
HGVS NC_000010.10:g.43615610C>T
CLNSRC
CLNACC RCV000461915.1,