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: rs1137070
rs1137070
9 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 0.030 1.000 3 2009 2016
dbSNP: rs1465107
rs1465107
1 1.000 0.040 X 43678769 intron variant A/G snv 0.010 1.000 1 2010 2010
dbSNP: rs2072743
rs2072743
1 1.000 0.040 X 43740274 intron variant T/C snv 0.010 1.000 1 2010 2010
dbSNP: rs6323
rs6323
7 0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 0.010 1.000 1 2010 2010