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: rs11013962
rs11013962
1 10 24206657 intron variant A/G snv 0.48 0.700 1.000 1 2010 2010
dbSNP: rs2270447
rs2270447
1 2 162103238 intergenic variant T/C snv 0.11 0.700 1.000 1 2010 2010
dbSNP: rs1057516029
rs1057516029
6 0.882 0.160 5 14290809 stop gained G/T snv 0.700 0