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: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.890 0.900 10 2010 2019
dbSNP: rs493258
rs493258
3 0.925 0.040 15 58395681 intron variant T/C snv 0.50 0.860 1.000 7 2010 2019
dbSNP: rs920915
rs920915
2 1.000 0.040 15 58396268 intron variant C/G snv 0.55 0.810 1.000 2 2013 2019
dbSNP: rs2043085
rs2043085
9 0.827 0.080 15 58388755 intron variant T/C snv 0.54 0.710 1.000 2 2016 2019
dbSNP: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.710 1.000 2 2016 2019