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: rs2274316
rs2274316
3 0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54 0.820 0.500 4 2012 2017
dbSNP: rs1925950
rs1925950
1 1 156480948 missense variant G/A;C snv 0.62 0.800 1.000 2 2012 2016
dbSNP: rs3790455
rs3790455
1 1 156486509 intron variant C/T snv 0.54 0.800 1.000 2 2012 2013
dbSNP: rs202206511
rs202206511
1 1 156486509 intron variant -/T delins 0.700 1.000 2 2012 2013
dbSNP: rs1050316
rs1050316
3 1 156464911 3 prime UTR variant G/T snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs2274319
rs2274319
2 1 156481081 intron variant T/C snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs3790459
rs3790459
1 1 156491915 intron variant A/T snv 0.54 0.700 1.000 1 2012 2012