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: rs4810426
rs4810426
1 1.000 0.080 20 44373081 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs4812831
rs4812831
1 1.000 0.080 20 44389620 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs2425637
rs2425637
3 0.925 0.080 20 44395409 intron variant G/T snv 0.42 0.010 < 0.001 1 2010 2010