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: rs1160351
rs1160351
2 1.000 0.040 14 47546779 intron variant A/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs13202860
rs13202860
2 1.000 0.040 6 86445536 intergenic variant A/T snv 6.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs13436218
rs13436218
2 1.000 0.040 5 129664693 intron variant T/G snv 1.0E-01 0.700 1.000 1 2012 2012
dbSNP: rs225848
rs225848
2 1.000 0.040 14 30125451 intron variant G/A snv 0.91 0.700 1.000 1 2012 2012