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: rs1570204
rs1570204
1 9 4216751 intron variant T/C snv 0.25 0.700 1.000 2 2018 2018
dbSNP: rs6476827
rs6476827
1 9 4220832 intron variant C/G snv 0.24 0.700 1.000 2 2018 2018
dbSNP: rs2224492
rs2224492
1 9 4237546 intron variant A/G snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs7047871
rs7047871
1 9 4050113 intron variant T/A snv 0.30 0.700 1.000 1 2019 2019