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rs121913312

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GAGCTG;GAGCTG) 0 common in clinvar
Make rs121913312(-;-)
Make rs121913312(-;GAGCTG)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position43114494
GeneRET
is asnp
is mentioned by
dbSNPrs121913312
dbSNP (old)rs121913312
ClinGenrs121913312
ebirs121913312
HLIrs121913312
Exacrs121913312
Gnomadrs121913312
Varsomers121913312
Maprs121913312
PheGenIrs121913312
Biobankrs121913312
1000 genomesrs121913312
hgdprs121913312
ensemblrs121913312
gopubmedrs121913312
geneviewrs121913312
scholarrs121913312
googlers121913312
pharmgkbrs121913312
gwascentralrs121913312
openSNPrs121913312
23andMers121913312
23andMe allrs121913312
SNPshotrs121913312
SNPdbers121913312
MSV3drs121913312
GWAS Ctlgrs121913312
Max Magnitude0
ClinVar
Risk rs121913312(-;-)
Alt rs121913312(-;-)
Reference Rs121913312(GAGCTG;GAGCTG)
Significance Probable-Pathogenic
Disease Medullary thyroid carcinoma
Variation info
Gene RET
CLNDBN Medullary thyroid carcinoma
Reversed 0
HGVS NC_000010.10:g.43609942_43609947delGAGCTG
CLNSRC
CLNACC RCV000438390.1,