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: rs10494747
rs10494747
1 1 197194798 intron variant A/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs10754218
rs10754218
2 1 197195884 intron variant G/A snv 0.60 0.700 1.000 1 2013 2013
dbSNP: rs10801596
rs10801596
1 1 197196137 intron variant G/A snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs10922177
rs10922177
1 1 197184637 intron variant T/C snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs1127661
rs1127661
1 1 197153913 3 prime UTR variant T/C snv 0.30 0.700 1.000 1 2013 2013
dbSNP: rs12028827
rs12028827
1 1 197158361 3 prime UTR variant A/C snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs12128631
rs12128631
1 1 197159596 synonymous variant G/A;C snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs12137359
rs12137359
1 1 197160851 intron variant C/T snv 0.17 0.700 1.000 1 2013 2013
dbSNP: rs4244139
rs4244139
1 1 197162244 intron variant G/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs4639796
rs4639796
1 1 197157519 3 prime UTR variant G/A snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs6677930
rs6677930
1 1 197166336 intron variant C/A snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs6690022
rs6690022
1 1 197200897 upstream gene variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs7410943
rs7410943
2 1 197185891 intron variant A/G snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs7516246
rs7516246
1 1 197196582 intron variant C/T snv 0.63 0.700 1.000 1 2013 2013