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: rs7850258
rs7850258
0.827 0.200 9 97786731 intron variant A/G snv 0.72
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.820 1.000 2 2011 2019
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: rs1588635
rs1588635
1.000 0.080 9 97775520 intron variant A/C snv 0.72
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.800 1.000 1 2010 2017
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
Thyroid stimulating hormone measurement
0.800 1.000 1 2014 2014
dbSNP: rs1867277
rs1867277
0.776 0.160 9 97853632 5 prime UTR variant A/G snv 0.63
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.750 1.000 1 2009 2015
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.710 1.000 2 2011 2014
dbSNP: rs7850258
rs7850258
0.827 0.200 9 97786731 intron variant A/G snv 0.72
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.710 1.000 2 2010 2015
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.700 1.000 3 2009 2013
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: rs10739496
rs10739496
9 97790277 intron variant C/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10818050
rs10818050
9 97776641 intron variant A/G;T snv
Thyroid stimulating hormone measurement
0.700 1.000 1 2014 2014
dbSNP: rs10818050
rs10818050
9 97776641 intron variant A/G;T snv
Blood thyroid stimulating hormone analysis
0.700 1.000 1 2014 2014
dbSNP: rs10818090
rs10818090
9 97799204 intron variant C/T snv 0.73
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10983700
rs10983700
1.000 0.080 9 97775173 intron variant T/A;C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10983700
rs10983700
1.000 0.080 9 97775173 intron variant T/A;C snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.700 1.000 1 2010 2010
dbSNP: rs10983701
rs10983701
9 97775295 intron variant G/A snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10983761
rs10983761
9 97791675 intron variant A/C;G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs12348691
rs12348691
0.925 0.120 9 97846400 intron variant G/A snv 0.63
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.700 1.000 1 2013 2013
dbSNP: rs1443438
rs1443438
0.827 0.080 9 97787746 intron variant T/A;C snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2012 2012
dbSNP: rs1443438
rs1443438
0.827 0.080 9 97787746 intron variant T/A;C snv
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.700 1.000 1 2013 2013
dbSNP: rs1443438
rs1443438
0.827 0.080 9 97787746 intron variant T/A;C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs1561962
rs1561962
9 97783937 intron variant C/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012