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: rs11214489
rs11214489
1 11 113105212 intron variant C/T snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs1273044
rs1273044
1 11 113123126 intron variant T/C;G snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs2288158
rs2288158
1 11 113262954 3 prime UTR variant T/G snv 0.15 0.13 0.700 1.000 1 2018 2018
dbSNP: rs78599561
rs78599561
1 11 113261790 intron variant T/A snv 0.13 0.700 1.000 1 2018 2018