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: rs16879552
rs16879552
3 0.882 0.080 8 32553698 intron variant C/T snv 0.10 0.850 0.833 6 2009 2019
dbSNP: rs7005606
rs7005606
3 0.925 0.080 8 32543983 intron variant T/G snv 0.39 0.700 1.000 2 2014 2016
dbSNP: rs7835688
rs7835688
2 0.925 0.080 8 32553981 intron variant G/A;C;T snv 0.050 0.800 5 2014 2019
dbSNP: rs2439302
rs2439302
9 0.776 0.200 8 32574851 intron variant G/C snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs2439305
rs2439305
1 1.000 0.080 8 32571946 intron variant G/A snv 0.54 0.010 1.000 1 2012 2012
dbSNP: rs7834206
rs7834206
1 1.000 0.080 8 32548630 5 prime UTR variant C/A;G snv 0.010 1.000 1 2018 2018