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: rs4409766
rs4409766
6 1.000 0.040 10 102856906 intron variant T/C snv 0.14 0.700 1.000 2 2017 2018
dbSNP: rs12765002
rs12765002
2 1.000 0.040 10 102875591 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs77335224
rs77335224
1 10 102876519 intron variant C/A;T snv 0.11 0.700 1.000 1 2019 2019