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: rs7754840
rs7754840
8 0.807 0.200 6 20661019 intron variant G/A;C;T snv 0.890 0.889 9 2009 2019
dbSNP: rs7756992
rs7756992
9 0.827 0.240 6 20679478 intron variant A/G;T snv 0.030 1.000 3 2009 2018
dbSNP: rs6935599
rs6935599
1 1.000 0.080 6 20716864 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs6938256
rs6938256
1 6 20887723 intron variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs7747752
rs7747752
1 1.000 0.080 6 20725192 intron variant G/C snv 0.34 0.010 1.000 1 2019 2019
dbSNP: rs9350276
rs9350276
1 1.000 0.080 6 20740065 intron variant C/T snv 0.38 0.010 1.000 1 2019 2019