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: rs6584555
rs6584555
1 1.000 0.080 10 103539854 intron variant T/C snv 0.27 0.740 0.800 5 2016 2019
dbSNP: rs11598047
rs11598047
1 1.000 0.080 10 103582915 non coding transcript exon variant A/G snv 0.16 0.700 1.000 3 2017 2018
dbSNP: rs60572254
rs60572254
1 1.000 0.080 10 103565017 intron variant C/T snv 0.700 1.000 2 2017 2018
dbSNP: rs55693294
rs55693294
1 1.000 0.080 10 103517717 intron variant C/T snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs60848348
rs60848348
1 1.000 0.080 10 103562124 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017