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: rs4880
rs4880
131 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 0.020 1.000 2 2010 2010
dbSNP: rs1165109290
rs1165109290
2 0.925 0.080 6 159692850 synonymous variant G/A snv 4.2E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs2758339
rs2758339
2 0.925 0.080 6 159691552 3 prime UTR variant A/C;T snv 0.010 1.000 1 2020 2020
dbSNP: rs5746136
rs5746136
6 0.807 0.200 6 159682052 3 prime UTR variant C/T snv 0.27 0.010 1.000 1 2020 2020