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: rs1443438
rs1443438
PTCSC2
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
PTCSC2
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
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012