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: rs2814778
rs2814778
24 0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 0.800 1.000 5 2012 2019
dbSNP: rs12075
rs12075
22 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 0.800 1.000 3 2011 2019
dbSNP: rs34599082
rs34599082
8 1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 0.700 1.000 2 2016 2019
dbSNP: rs3027001
rs3027001
3 1.000 0.040 1 159199673 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs3027012
rs3027012
3 1 159204333 5 prime UTR variant C/T snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs7550207
rs7550207
5 1 159205095 intron variant T/C snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs863002
rs863002
2 1 159205130 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011