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: rs11634851
rs11634851
1 15 80736624 intron variant C/G snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs2062316
rs2062316
1 15 80717908 intron variant A/G snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs2759308
rs2759308
2 15 80723886 intron variant G/A snv 0.34 0.700 1.000 1 2017 2017
dbSNP: rs35175632
rs35175632
1 15 80745392 intron variant TT/-;T;TTT;TTTT delins 0.700 1.000 1 2019 2019
dbSNP: rs35199222
rs35199222
1 15 80720696 intron variant G/A snv 0.32 0.700 1.000 1 2017 2017