Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs77558292
rs77558292
RET
0.710 GeneticVariation BEFREE Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C609R; n=1) and 13 (Y791F, n=3) had sporadic short-segment HD with normal thyroid US and serum calcitonin. 23744765

2013
dbSNP: rs77558292
rs77558292
RET
C 0.710 GeneticVariation CLINVAR