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: rs780159
rs780159
2 10 79147390 intron variant A/C;G snv 0.700 1.000 2 2018 2019
dbSNP: rs703984
rs703984
1 10 79181660 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs779933
rs779933
2 10 79158760 intron variant G/A snv 0.36 0.700 1.000 1 2019 2019