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: rs12967855
rs12967855
2 1.000 0.040 18 37558282 intron variant A/G snv 0.52 0.700 1.000 2 2018 2019
dbSNP: rs11082011
rs11082011
3 0.925 0.040 18 37565159 intron variant C/T snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs11877758
rs11877758
1 1.000 0.040 18 37558147 intron variant T/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs4799936
rs4799936
1 1.000 0.040 18 37524865 intron variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs80035064
rs80035064
2 1.000 0.040 18 37566403 intron variant T/A snv 0.18 0.700 1.000 1 2018 2018