Source: GWASCAT ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12124523
rs12124523
2 1.000 0.040 1 72155780 intron variant C/T snv 7.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs1620977
rs1620977
3 1.000 0.040 1 72263459 intron variant A/G;T snv 0.700 1.000 1 2018 2018