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: rs2238368
rs2238368
4 16 120329 intron variant C/T snp 0.37 0.800 2 2012 2017
dbSNP: rs7203560
rs7203560
8 1.000 0.071 16 134391 intron variant T/G snp 1.9E-02 0.800 2 2013 2017
dbSNP: rs11248850
rs11248850
2 16 113599 intron variant G/A snp 0.38 0.800 1 2012 2012
dbSNP: rs117747069
rs117747069
5 16 120077 intron variant G/C snp 2.2E-02 0.700 1 2017 2017
dbSNP: rs11865131
rs11865131
2 16 113668 intron variant G/A snp 0.38 0.700 1 2012 2012
dbSNP: rs12927713
rs12927713
2 16 102222 intron variant G/A snp 0.39 0.700 1 2012 2012
dbSNP: rs183350
rs183350
2 16 111939 intron variant G/A snp 0.80 0.700 1 2012 2012
dbSNP: rs216093
rs216093
2 16 114936 intron variant T/G snp 0.88 0.700 1 2012 2012
dbSNP: rs2541618
rs2541618
2 16 92827 non coding transcript exon variant T/C snp 0.83 0.700 1 2012 2012
dbSNP: rs2562164
rs2562164
2 16 126744 intron variant A/G snp 0.31 0.700 1 2012 2012
dbSNP: rs2562177
rs2562177
2 16 95284 intron variant C/T snp 5.8E-02 0.700 1 2012 2012
dbSNP: rs2562181
rs2562181
2 16 91661 intron variant C/T snp 0.12 0.700 1 2012 2012
dbSNP: rs2562189
rs2562189
2 16 137430 intron variant C/A,T snp 0.51 0.700 1 2012 2012
dbSNP: rs2857997
rs2857997
2 16 135103 intron variant G/C snp 0.52 0.700 1 2012 2012
dbSNP: rs2857998
rs2857998
2 16 135124 intron variant A/G snp 0.52 0.700 1 2012 2012
dbSNP: rs545105162
rs545105162
2 16 98445 intron variant G/A snp 7.4E-04 0.700 1 2017 2017
dbSNP: rs6600233
rs6600233
3 16 93505 intron variant C/G,T snp 3.2E-05; 0.34 0.700 1 2012 2012
dbSNP: rs7199157
rs7199157
2 16 105968 intron variant C/G snp 0.39 0.700 1 2012 2012
dbSNP: rs743725
rs743725
2 16 86889 intron variant T/A,C snp 4.2E-06; 0.80 0.74 0.700 1 2012 2012
dbSNP: rs798604
rs798604
2 16 118692 intron variant C/A,G snp 9.6E-05; 0.15 0.700 1 2012 2012
dbSNP: rs798613
rs798613
2 16 104846 intron variant C/T snp 7.7E-02 0.700 1 2012 2012