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: rs1106766
rs1106766
7 0.882 0.120 12 57415673 intron variant C/T snv 0.19 0.700 1.000 2 2010 2013
dbSNP: rs11172147
rs11172147
2 0.925 0.120 12 57302894 intron variant G/A snv 0.19 0.700 1.000 2 2010 2013
dbSNP: rs11609805
rs11609805
2 0.925 0.120 12 57341262 5 prime UTR variant G/A;C;T snv 0.700 1.000 2 2010 2013
dbSNP: rs11613352
rs11613352
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.700 1.000 2 2010 2013
dbSNP: rs11614506
rs11614506
2 0.925 0.120 12 57421892 intron variant T/C snv 0.16 0.700 1.000 2 2010 2013
dbSNP: rs4760254
rs4760254
2 0.925 0.120 12 57372609 intron variant G/A;C;T snv 0.700 1.000 2 2010 2013
dbSNP: rs4760278
rs4760278
2 0.925 0.120 12 57377370 intron variant C/A snv 0.16 0.700 1.000 2 2010 2013
dbSNP: rs4760355
rs4760355
3 0.925 0.120 12 57331414 intron variant G/A snv 0.20 0.700 1.000 2 2010 2013
dbSNP: rs7964492
rs7964492
2 0.925 0.120 12 57429802 intron variant A/C snv 0.19 0.700 1.000 2 2010 2013