Source: GWASCAT

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: rs1352714
rs1352714
DCHS2
0.925 0.280 4 154322452 missense variant T/C snv 0.95 0.90
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.700 1.000 1 2019 2019
dbSNP: rs1352714
rs1352714
DCHS2
0.925 0.280 4 154322452 missense variant T/C snv 0.95 0.90
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
Thyrotoxic periodic paralysis 		0.700 1.000 1 2019 2019