Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1364709483
rs1364709483
TBX2 ; TBX2-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555939456
rs1555939456
RPS6KA3
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267608327
rs267608327
MECP2
T 0.700 CausalMutation CLINVAR

dbSNP: rs2281135
rs2281135
PNPLA3
0.010 GeneticVariation BEFREE Three SNP-diagnosis pairs passed the phenome-wide significance threshold: rs9273349 and E06 (thyroiditis, p = 5.50x10-8); rs9273349 and E10 (type-1 diabetes, p = 2.60x10-7); and rs2281135 and K76 (non-alcoholic liver diseases, including NAFLD, p = 4.10x10-7). 30978214

2019
dbSNP: rs9273349
rs9273349
HLA-DQB1-AS1
0.010 GeneticVariation BEFREE Three SNP-diagnosis pairs passed the phenome-wide significance threshold: rs9273349 and E06 (thyroiditis, p = 5.50x10-8); rs9273349 and E10 (type-1 diabetes, p = 2.60x10-7); and rs2281135 and K76 (non-alcoholic liver diseases, including NAFLD, p = 4.10x10-7). 30978214

2019
dbSNP: rs113488022
rs113488022
BRAF
0.010 GeneticVariation BEFREE The presence of BRAF V600E was only associated with extrathyroidal extension and the absence of thyroiditis. 25266729

2014
dbSNP: rs121913377
rs121913377
BRAF
0.010 GeneticVariation BEFREE The presence of BRAF V600E was only associated with extrathyroidal extension and the absence of thyroiditis. 25266729

2014