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: rs10097731
rs10097731
1 8 81115437 upstream gene variant G/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs1260326
rs1260326
81 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 0.700 1.000 1 2012 2012
dbSNP: rs204999
rs204999
13 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs2280401
rs2280401
5 19 49496752 intron variant G/A snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs3777200
rs3777200
1 5 95899087 intron variant C/T snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs4561508
rs4561508
3 17 16945436 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012