Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12484776
rs12484776
TNRC6B
1.000 22 40256869 intron variant A/G snv 0.19
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids 		0.820 1.000 1 2011 2018
dbSNP: rs139909
rs139909
TNRC6B
22 40301577 intron variant C/T snv 0.74
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2009 2009
dbSNP: rs9623117
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs9623117
rs9623117
TNRC6B
0.851 0.200 22 40056115 intron variant T/C snv 0.38
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.700 1.000 1 2009 2009