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: rs6592965
rs6592965
4 7 50360284 intron variant G/A snv 0.47 0.700 1.000 3 2016 2019
dbSNP: rs12534526
rs12534526
2 7 50358399 intron variant G/A snv 0.32 0.700 1.000 1 2009 2009
dbSNP: rs12669559
rs12669559
3 1.000 0.120 7 50368079 synonymous variant T/G snv 0.35 0.32 0.700 1.000 1 2009 2009
dbSNP: rs12718598
rs12718598
3 7 50360747 intron variant T/C snv 0.50 0.700 1.000 1 2009 2009
dbSNP: rs7385935
rs7385935
2 7 50363173 intron variant G/A snv 0.35 0.700 1.000 1 2009 2009