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: rs1042779
rs1042779
4 0.882 0.040 3 52786995 missense variant A/G snv 0.40 0.42 0.700 1.000 1 2013 2013
dbSNP: rs2239549
rs2239549
1 1.000 0.040 3 52789110 intron variant G/A snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs2239551
rs2239551
1 1.000 0.040 3 52784563 intron variant G/A snv 0.33 0.700 1.000 1 2013 2013
dbSNP: rs2286798
rs2286798
2 1.000 0.040 3 52787161 intron variant A/C snv 0.38 0.37 0.700 1.000 1 2013 2013
dbSNP: rs2300149
rs2300149
2 1.000 0.040 3 52788905 intron variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs3774354
rs3774354
3 0.882 0.080 3 52783659 intron variant G/A snv 0.31 0.700 1.000 1 2013 2013