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: rs16951275
rs16951275
2 15 67784830 intron variant T/C snv 0.30 0.700 1.000 4 2015 2019
dbSNP: rs2241423
rs2241423
7 0.882 0.120 15 67794500 intron variant G/A snv 0.29 0.700 1.000 4 2010 2019
dbSNP: rs4776970
rs4776970
4 15 67788548 intron variant A/T snv 0.44 0.700 1.000 4 2012 2018
dbSNP: rs11637027
rs11637027
1 15 67645417 intron variant G/T snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs28376010
rs28376010
1 15 67771401 intron variant G/T snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs3784710
rs3784710
2 15 67780120 intron variant T/C snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs3865018
rs3865018
1 15 67600428 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs7175517
rs7175517
2 15 67785292 intron variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs8025790
rs8025790
2 15 67784061 intron variant G/T snv 0.30 0.700 1.000 1 2017 2017