Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518799
rs1057518799
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518891
rs1057518891
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057523354
rs1057523354
A 0.700 CausalMutation CLINVAR

dbSNP: rs1085308047
rs1085308047
G 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
T 0.700 GeneticVariation CLINVAR

dbSNP: rs142698837
rs142698837
TG
A 0.700 CausalMutation CLINVAR

dbSNP: rs1553769428
rs1553769428
HJV
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555570093
rs1555570093
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1562203136
rs1562203136
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1567498374
rs1567498374
A 0.700 CausalMutation CLINVAR

dbSNP: rs28939701
rs28939701
A 0.700 CausalMutation CLINVAR

dbSNP: rs387907141
rs387907141
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507531
rs397507531
C 0.700 CausalMutation CLINVAR

dbSNP: rs587777630
rs587777630
A 0.700 CausalMutation CLINVAR

dbSNP: rs72653706
rs72653706
A 0.700 CausalMutation CLINVAR

dbSNP: rs74799832
rs74799832
RET
C 0.700 CausalMutation CLINVAR

dbSNP: rs752746786
rs752746786
G 0.700 CausalMutation CLINVAR

dbSNP: rs770374710
rs770374710
TG 0.700 CausalMutation CLINVAR

dbSNP: rs794727931
rs794727931
C 0.700 CausalMutation CLINVAR

dbSNP: rs866294686
rs866294686
T 0.700 GeneticVariation CLINVAR

dbSNP: rs876661024
rs876661024
A 0.700 CausalMutation CLINVAR

dbSNP: rs886041116
rs886041116
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121908862
rs121908862
0.010 GeneticVariation BEFREE After the finding of partial loss-of-function mutations leading to hyperthyrotropinemia (Sunthornthepvarakul et al., 1995) it was speculated that a more severe phenotype with hypothyroidism and hypoplasia of the gland (thyroid dysgenesis) would be the result, if complete loss-of-function mutations like the isoleucine167 to asparagine mutation would occur in a homozygote or compound heterozygote state. 8981017

1996

dbSNP: rs2076738
rs2076738
TG
0.010 GeneticVariation BEFREE Missense mutation (C1263R) in the thyroglobulin gene causes congenital goiter with mild hypothyroidism by impaired intracellular transport. 9790265

1998

dbSNP: rs121908866
rs121908866
0.010 GeneticVariation BEFREE The W546X allele was detected in approximately 1 in 180 individuals and may be a major contributor to hypothyroidism in the Welsh population. 12629076

2003