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: rs987237
rs987237
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.700 1.000 5 2010 2019
dbSNP: rs2206277
rs2206277
4 0.925 0.080 6 50830813 intron variant C/T snv 0.19 0.700 1.000 3 2015 2019
dbSNP: rs2206271
rs2206271
3 6 50818295 upstream gene variant T/A snv 0.32 0.700 1.000 1 2017 2017