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: rs11778040
rs11778040
1 1.000 0.040 8 27562290 intron variant C/T snv 0.19 0.700 1.000 2 2017 2019
dbSNP: rs59724122
rs59724122
2 0.925 0.040 8 27567179 intron variant C/T snv 0.13 0.700 1.000 2 2018 2019
dbSNP: rs73229090
rs73229090
1 1.000 0.040 8 27584610 intron variant C/A snv 7.7E-02 0.700 1.000 2 2014 2015
dbSNP: rs11783093
rs11783093
2 1.000 0.040 8 27567832 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018