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rs77724903

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs77724903(A;T)
Make rs77724903(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position43118460
GeneRET
is asnp
is mentioned by
dbSNPrs77724903
ebirs77724903
HLIrs77724903
Exacrs77724903
Varsomers77724903
Maprs77724903
PheGenIrs77724903
hapmaprs77724903
1000 genomesrs77724903
hgdprs77724903
ensemblrs77724903
gopubmedrs77724903
geneviewrs77724903
scholarrs77724903
googlers77724903
pharmgkbrs77724903
gwascentralrs77724903
openSNPrs77724903
23andMers77724903
23andMe allrs77724903
SNP Nexus

SNPshotrs77724903
SNPdbers77724903
MSV3drs77724903
GWAS Ctlgrs77724903
Max Magnitude0
OMIM164761
Desc
Variant0034
Relatedalso
ClinVar
Risk rs77724903(T;T)
Alt rs77724903(T;T)
Reference rs77724903(A;A)
Significance Other
Disease Familial medullary thyroid carcinoma Pheochromocytoma MEN2A and FMTC not provided Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome Hirschsprung's disease not specified
Variation info
Gene RET
CLNDBN Familial medullary thyroid carcinoma Pheochromocytoma MEN2A and FMTC not provided Multiple endocrine neoplasia, type 2 Hereditary cancer-predisposing syndrome Hirschsprung's disease not specified
Reversed 0
HGVS NC_000010.10:g.43613908A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000014962.26, RCV000014963.26, RCV000021851.1, RCV000034771.4, RCV000123309.5, RCV000130367.2, RCV000148769.1, RCV000235206.1,


[PMID 12000816] Germ-line mutations in nonsyndromic pheochromocytoma.


[PMID 16118333] Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?