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: rs10101067
rs10101067
2 8 71495139 intron variant G/C snv 6.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs12549058
rs12549058
1 8 71580003 intron variant T/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs28446899
rs28446899
1 8 71483978 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs4738141
rs4738141
3 8 71557507 intron variant A/G snv 0.41 0.700 1.000 1 2018 2018
dbSNP: rs6994124
rs6994124
1 8 71580950 intron variant T/A;C;G snv 0.700 1.000 1 2019 2019