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: rs1588635
rs1588635
PTCSC2
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: rs1588635
rs1588635
PTCSC2
1.000 0.080 9 97775520 intron variant A/C snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012