Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1370328347
CSH1
1.000 0.080 17 63895621 missense variant C/A;T snv 1.0E-05; 1.0E-05 1
rs767816037
CSH2
1.000 0.080 17 63872725 missense variant C/G;T snv 4.5E-05 1
rs775020499
LRSAM1
1.000 0.080 9 127467764 missense variant A/G snv 8.2E-06 1
rs1050851
NFKBIA
1.000 0.080 14 35403720 synonymous variant G/A snv 0.17 0.15 1
rs2233417
NFKBIA
1.000 0.080 14 35402888 intron variant C/T snv 0.14 0.13 1
rs1955656
SERPINA5
1.000 0.080 14 94579038 intron variant G/A snv 0.14 1
rs2093266
SERPINA5 ; SERPINA4
1.000 0.080 14 94566450 intron variant G/A snv 0.15 1