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rs267607011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607011(C;G)
Make rs267607011(G;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position43120184
GeneRET
is asnp
is mentioned by
dbSNPrs267607011
ebirs267607011
HLIrs267607011
Exacrs267607011
Varsomers267607011
Maprs267607011
PheGenIrs267607011
hapmaprs267607011
1000 genomesrs267607011
hgdprs267607011
ensemblrs267607011
gopubmedrs267607011
geneviewrs267607011
scholarrs267607011
googlers267607011
pharmgkbrs267607011
gwascentralrs267607011
openSNPrs267607011
23andMers267607011
23andMe allrs267607011
SNP Nexus

SNPshotrs267607011
SNPdbers267607011
MSV3drs267607011
GWAS Ctlgrs267607011
Max Magnitude0
ClinVar
Risk rs267607011(G,T;G,T)
Alt rs267607011(G,T;G,T)
Reference rs267607011(C;C)
Significance Pathogenic
Disease Multiple endocrine neoplasia MEN2 phenotype: Unknown MEN2 phenotype: Unclassified
Variation info
Gene RET
CLNDBN Multiple endocrine neoplasia, type 2b MEN2 phenotype: Unknown MEN2 phenotype: Unclassified
Reversed 0
HGVS NC_000010.10:g.43615632C>G; NC_000010.10:g.43615632C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014972.25, RCV000021877.1, RCV000021878.1,


[PMID 17895320] RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.