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: rs13283416
rs13283416
2 1.000 0.040 9 116539328 intron variant T/G snv 0.41 0.700 1.000 2 2019 2019
dbSNP: rs10983324
rs10983324
1 9 116723058 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1321917
rs1321917
1 9 116562650 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs13298297
rs13298297
2 9 116501829 intron variant G/A snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs4836732
rs4836732
2 1.000 0.040 9 116504416 intron variant C/T snv 0.49 0.700 1.000 1 2019 2019