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: rs10197140
rs10197140
3 2 110852366 intron variant T/C snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs2009581
rs2009581
3 2 111050100 intron variant G/A snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs4848370
rs4848370
2 2 111054088 intron variant C/T snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs4849121
rs4849121
3 0.925 0.160 2 110842129 intron variant G/A snv 0.44 0.700 1.000 1 2019 2019