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: rs7850258
rs7850258
PTCSC2
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: rs7850258
rs7850258
PTCSC2
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: rs7850258
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012