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: rs2282978
rs2282978
5 7 92635096 intron variant T/C snv 0.38 0.700 1.000 3 2008 2009
dbSNP: rs42039
rs42039
3 1.000 0.080 7 92615108 3 prime UTR variant C/T snv 0.19 0.19 0.700 1.000 2 2014 2019
dbSNP: rs42235
rs42235
2 7 92618762 intron variant C/T snv 0.32 0.700 1.000 2 2010 2013
dbSNP: rs42377
rs42377
3 7 92614358 3 prime UTR variant G/A snv 0.28 0.700 1.000 2 2017 2019
dbSNP: rs2040494
rs2040494
3 7 92627591 intron variant C/T snv 0.64 0.700 1.000 1 2008 2008
dbSNP: rs3731267
rs3731267
1 7 92831361 intron variant C/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs3731321
rs3731321
1 7 92698451 intron variant T/C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs445
rs445
9 7 92779056 intron variant C/T snv 0.14 0.700 1.000 1 2019 2019