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: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 1 2011 2011
dbSNP: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs2043085
rs2043085
9 0.827 0.080 15 58388755 intron variant T/C snv 0.54 0.800 1.000 1 2011 2011
dbSNP: rs11631342
rs11631342
1 1.000 0.040 15 58432184 non coding transcript exon variant A/G snv 5.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs16940170
rs16940170
2 1.000 0.040 15 58392083 intron variant G/A snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs16940212
rs16940212
4 1.000 0.040 15 58401821 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs495348
rs495348
2 1.000 0.040 15 58395591 intron variant C/G snv 0.82 0.700 1.000 1 2018 2018
dbSNP: rs6494005
rs6494005
5 1.000 0.040 15 58432325 non coding transcript exon variant A/G snv 0.38 0.700 1.000 1 2018 2018