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: rs9494457
rs9494457
2 1.000 0.040 6 136153656 intron variant T/A snv 0.39 0.700 1.000 3 2018 2018
dbSNP: rs4896199
rs4896199
1 6 136144434 intron variant A/C;T snv 0.700 1.000 1 2018 2018