Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs212099
rs212099
19 47885745 intron variant T/A snv 0.12
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs2547231
rs2547231
19 47881800 intron variant C/A snv 0.86
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs2910393
rs2910393
19 47877871 intron variant T/A;C snv
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011
dbSNP: rs296365
rs296365
19 47871294 3 prime UTR variant C/A;G snv
CUI: C0441683
Disease: Hormone measurement
Hormone measurement
0.700 1.000 1 2011 2011