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: rs10748842
rs10748842
8 0.807 0.120 10 81889983 intron variant T/C snv 0.13 0.010 1.000 1 2017 2017
dbSNP: rs10883866
rs10883866
3 0.882 0.160 10 81883883 intron variant C/A;G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs6584400
rs6584400
6 0.851 0.120 10 81896770 intron variant G/A snv 0.22 0.010 1.000 1 2017 2017