Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs826220
rs826220
THRB
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs869422
rs869422
ZMAT4
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs9585327
rs9585327 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs9747347
rs9747347
NPLOC4 ; TSPAN10
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs9866391
rs9866391
PXYLP1 ; ZBTB38
0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965

2016
dbSNP: rs10113215
rs10113215 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373

2014
dbSNP: rs1064795104
rs1064795104
EXOC6B
C 0.700 GeneticVariation CLINVAR Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability. 25256811

2014
dbSNP: rs1370156
rs1370156 		0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. 25233373

2014
dbSNP: rs1064795104
rs1064795104
EXOC6B
C 0.700 GeneticVariation CLINVAR Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. 23422942

2013
dbSNP: rs1057518799
rs1057518799
POGZ
TGATTGGCA 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518812
rs1057518812
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518829
rs1057518829
CACNA1F
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518848
rs1057518848
TCF4
CATTG 0.700 CausalMutation CLINVAR

dbSNP: rs1057518881
rs1057518881
FBN1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518891
rs1057518891
CHD7
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518909
rs1057518909
FBN1
C 0.700 CausalMutation CLINVAR

dbSNP: rs1057518938
rs1057518938
MYH11 ; NDE1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307138
rs1085307138
PUF60 ; SCRIB
T 0.700 GeneticVariation CLINVAR

dbSNP: rs111854391
rs111854391
TGFBR1
T 0.700 CausalMutation CLINVAR

dbSNP: rs113422242
rs113422242
FBN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121912683
rs121912683
SLC25A4
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121912882
rs121912882
COL2A1 ; LOC105369752
A 0.700 CausalMutation CLINVAR

dbSNP: rs1294950721
rs1294950721
JAG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1331463984
rs1331463984
TRAF7
A 0.700 CausalMutation CLINVAR

dbSNP: rs142239530
rs142239530
STIM1
T 0.700 GeneticVariation CLINVAR