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: rs925489
rs925489
0.882 0.080 9 97784318 intron variant C/T snv 0.71
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.800 1.000 2 2011 2012
dbSNP: rs925489
rs925489
0.882 0.080 9 97784318 intron variant C/T snv 0.71
Thyroid stimulating hormone measurement
0.800 1.000 1 2014 2014
dbSNP: rs925489
rs925489
0.882 0.080 9 97784318 intron variant C/T snv 0.71
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.800 1.000 1 2010 2018
dbSNP: rs925489
rs925489
0.882 0.080 9 97784318 intron variant C/T snv 0.71
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs925489
rs925489
0.882 0.080 9 97784318 intron variant C/T snv 0.71
Blood thyroid stimulating hormone analysis
0.700 1.000 1 2014 2014