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: rs965513
rs965513
0.742 0.200 9 97793827 intron variant A/G;T snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.860 1.000 4 2009 2016
dbSNP: rs965513
rs965513
0.742 0.200 9 97793827 intron variant A/G;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 2 2011 2012
dbSNP: rs965513
rs965513
0.742 0.200 9 97793827 intron variant A/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs965513
rs965513
0.742 0.200 9 97793827 intron variant A/G;T snv
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma
0.700 1.000 1 2010 2010