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: rs7811417
rs7811417
SP4
1 1.000 0.040 7 21494534 intron variant T/C snv 0.70 0.700 1.000 2 2017 2019
dbSNP: rs73060317
rs73060317
SP4
1 1.000 0.040 7 21480594 intron variant T/G snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs10272006
rs10272006
SP4
3 0.925 0.080 7 21480514 intron variant G/A snv 0.75 0.010 1.000 1 2018 2018
dbSNP: rs12673091
rs12673091
SP4
1 1.000 0.040 7 21498449 intron variant A/G snv 0.36 0.010 1.000 1 2018 2018
dbSNP: rs2237304
rs2237304
SP4
1 1.000 0.040 7 21459475 intron variant T/A snv 0.21 0.010 1.000 1 2018 2018
dbSNP: rs2282888
rs2282888
SP4
1 1.000 0.040 7 21436514 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs40245
rs40245
SP4
2 1.000 0.040 7 21430918 intron variant A/T snv 0.73 0.010 1.000 1 2016 2016
dbSNP: rs6461563
rs6461563
SP4
1 1.000 0.040 7 21456779 intron variant G/A;T snv 0.010 1.000 1 2016 2016