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: rs61759532
rs61759532
1.000 0.040 17 7337072 intron variant C/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs61759532
rs61759532
1.000 0.040 17 7337072 intron variant C/A;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.700 1.000 1 2019 2019