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: rs303937
rs303937
1 13 71798392 intron variant T/A snv 0.51 0.700 1.000 2 2019 2019
dbSNP: rs626277
rs626277
5 1.000 0.080 13 71773564 intron variant A/C snv 0.51 0.700 1.000 2 2016 2018
dbSNP: rs9529913
rs9529913
2 13 71770957 intron variant C/A;T snv 0.700 1.000 2 2017 2019
dbSNP: rs487107
rs487107
1 13 71795027 intron variant G/T snv 0.51 0.700 1.000 1 2019 2019
dbSNP: rs500830
rs500830
1 13 71774636 intron variant C/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs584480
rs584480
2 13 71771373 intron variant C/T snv 0.50 0.700 1.000 1 2019 2019
dbSNP: rs716877
rs716877
2 13 71773316 intron variant C/G snv 0.43 0.700 1.000 1 2016 2016