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: rs7203560
rs7203560
7 1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 0.700 1.000 2 2013 2019
dbSNP: rs11248850
rs11248850
2 16 113599 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs117747069
rs117747069
4 16 120077 intron variant G/C snv 2.5E-02 0.700 1.000 1 2016 2016
dbSNP: rs11865131
rs11865131
1 16 113668 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs12927713
rs12927713
1 16 102222 intron variant G/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs183350
rs183350
3 0.925 0.040 16 111939 intron variant G/A snv 0.81 0.700 1.000 1 2012 2012
dbSNP: rs216093
rs216093
1 16 114936 intron variant T/G snv 0.89 0.700 1.000 1 2012 2012
dbSNP: rs2238368
rs2238368
4 16 120329 intron variant C/T snv 0.36 0.700 1.000 1 2012 2012
dbSNP: rs2541618
rs2541618
1 16 92827 non coding transcript exon variant T/C snv 0.84 0.700 1.000 1 2012 2012
dbSNP: rs2562164
rs2562164
1 16 126744 intron variant A/G snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs2562177
rs2562177
1 16 95284 intron variant C/T snv 6.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs2562181
rs2562181
1 16 91661 intron variant C/T snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs2562189
rs2562189
1 16 137430 intron variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2857997
rs2857997
1 16 135103 intron variant G/C snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs2857998
rs2857998
1 16 135124 intron variant A/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs60992881
rs60992881
2 16 107595 intron variant AAAAAAAAA/-;A;AA;AAA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAAAA delins 0.38 0.700 1.000 1 2016 2016
dbSNP: rs6600233
rs6600233
3 16 93505 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7199157
rs7199157
1 16 105968 intron variant C/G snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs743725
rs743725
1 16 86889 intron variant T/A;C snv 4.2E-06; 0.80 0.700 1.000 1 2012 2012
dbSNP: rs798604
rs798604
1 16 118692 intron variant C/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs798613
rs798613
1 16 104846 intron variant C/T snv 8.3E-02 0.700 1.000 1 2012 2012