Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs778826879 16 30121948 missense variant C/G,T snp 1.2E-05; 8.0E-06 3.2E-05 3
rs9983925 21 45216929 intron variant C/T snp 0.46 3
rs4746172
VCL
10 74096084 intron variant C/T snp 0.72 3
rs530348521 22 38112559 missense variant G/A snp 6.5E-06 3
rs4719714 7 22721094 A/T snp 0.20 3
rs3771300 2 190970870 intron variant T/G snp 0.48 3
rs2053044 5 148825809 5 prime UTR variant A/G snp 0.59 3
rs11674595 2 101994530 intron variant T/C snp 0.26 3
rs757725417 2 86144399 C/G,T snp 4.0E-06; 4.0E-06 3
rs7016778 8 53237545 intron variant A/T snp 0.17 3
rs12675595 8 53255365 intergenic variant G/A snp 6.3E-02 3
rs121908586 4 54274869 missense variant T/A,C snp 3
rs4236167 6 15533720 intron variant C/T snp 0.47 3
rs763004980 3 128906139 missense variant G/A snp 1.2E-05 6.4E-05 2
rs150283105 3 128909410 missense variant C/T snp 7.2E-05 9.6E-05 2
rs4482737 4 47320173 synonymous variant T/C,G snp 0.99; 4.0E-06 0.97 2
rs2351299 4 47141348 intron variant G/T snp 0.21 2
rs3832300 4 47426318 3 prime UTR variant C/CT in-del 5.1E-02 2
rs3915512 3 197295369 intron variant A/G,T snp 0.26 2
rs1799921 5 63961638 missense variant T/C snp 9.4E-03 7.8E-03 2
rs1799920 5 63961656 missense variant C/G,T snp 3.2E-04 5.4E-04 2
rs368311455 1 53211185 missense variant C/T snp 3.2E-05 3.2E-05 2
rs760292725 17 10681145 missense variant T/C snp 2
rs751557097 1 53213431 missense variant G/C snp 2.8E-05 2
rs1464681682 21 6486334 T/C,G snp 2