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: rs114455101
rs114455101
2 1.000 0.040 6 32465853 intron variant T/G snv 0.700 1.000 1 2017 2017
dbSNP: rs138984909
rs138984909
2 1.000 0.040 6 32466042 intron variant A/G snv 0.700 1.000 1 2017 2017
dbSNP: rs149998036
rs149998036
2 1.000 0.040 6 32470272 intron variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs186229361
rs186229361
2 1.000 0.040 6 32468178 intron variant T/C snv 0.700 1.000 1 2017 2017