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: rs131654
rs131654
1 1.000 0.080 22 21562901 intron variant G/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs7444
rs7444
2 1.000 0.080 22 21622645 3 prime UTR variant T/C snv 0.32 0.700 1.000 3 2015 2017
dbSNP: rs131658
rs131658
1 1.000 0.080 22 21563337 intron variant C/G snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs2283790
rs2283790
3 0.882 0.120 22 21602364 intron variant A/G snv 0.21 0.700 1.000 1 2017 2017