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: rs2236519
rs2236519
2 20 46900932 intron variant G/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs1007330
rs1007330
1 20 46897482 intron variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs1206825
rs1206825
1 20 47129619 intron variant A/T snv 0.64 0.700 1.000 1 2019 2019
dbSNP: rs12481664
rs12481664
1 20 46923095 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3092781
rs3092781
1 20 47161314 non coding transcript exon variant T/C snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs4809604
rs4809604
1 20 46921850 intron variant T/G snv 0.46 0.700 1.000 1 2019 2019