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: rs4602861
rs4602861
1 8 105578478 intron variant A/G;T snv 0.700 1.000 2 2015 2017
dbSNP: rs4541868
rs4541868
1 8 105578477 intron variant C/A snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs4734879
rs4734879
2 8 105570896 intron variant A/G snv 0.31 0.700 1.000 1 2019 2019