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: rs7085104
rs7085104
2 1.000 0.040 10 102869116 intron variant A/G snv 0.35 0.800 1.000 2 2013 2019
dbSNP: rs11191419
rs11191419
2 1.000 0.040 10 102852578 intron variant T/A snv 0.36 0.710 1.000 4 2014 2017
dbSNP: rs11191424
rs11191424
1 1.000 0.040 10 102866129 intron variant G/A snv 0.36 0.700 1.000 2 2017 2019
dbSNP: rs1046778
rs1046778
4 0.851 0.160 10 102901727 3 prime UTR variant T/C snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs10883795
rs10883795
1 1.000 0.040 10 102894820 intron variant T/C snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs11191454
rs11191454
9 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs12244388
rs12244388
1 1.000 0.040 10 102880295 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12764899
rs12764899
4 1.000 0.040 10 102875346 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019