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rs121913308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913308(A;G)
Make rs121913308(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position43114492
GeneRET
is asnp
is mentioned by
dbSNPrs121913308
dbSNP (old)rs121913308
ClinGenrs121913308
ebirs121913308
HLIrs121913308
Exacrs121913308
Gnomadrs121913308
Varsomers121913308
Maprs121913308
PheGenIrs121913308
Biobankrs121913308
1000 genomesrs121913308
hgdprs121913308
ensemblrs121913308
gopubmedrs121913308
geneviewrs121913308
scholarrs121913308
googlers121913308
pharmgkbrs121913308
gwascentralrs121913308
openSNPrs121913308
23andMers121913308
23andMe allrs121913308
SNPshotrs121913308
SNPdbers121913308
MSV3drs121913308
GWAS Ctlgrs121913308
Max Magnitude0
ClinVar
Risk rs121913308(C;C) rs121913308(G;G) rs121913308(T;T)
Alt rs121913308(C;C) rs121913308(G;G) rs121913308(T;T)
Reference Rs121913308(A;A)
Significance Probable-Pathogenic
Disease MEN2 phenotype: Unknown Medullary thyroid carcinoma
Variation info
Gene RET
CLNDBN MEN2 phenotype: Unknown Medullary thyroid carcinoma
Reversed 0
HGVS NC_000010.10:g.43609940A>C; NC_000010.10:g.43609940A>G; NC_000010.10:g.43609940A>T
CLNSRC UniProtKB (protein)
CLNACC RCV000021813.1, RCV000021814.1, RCV000431229.1, RCV000021815.1,