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: rs210138
rs210138
5 0.851 0.240 6 33574761 intron variant A/G snv 0.19 0.700 1.000 1 2010 2010
dbSNP: rs210139
rs210139
1 1.000 0.120 6 33575632 intron variant A/C snv 0.45 0.700 1.000 1 2010 2010
dbSNP: rs513349
rs513349
2 1.000 0.120 6 33573942 intron variant A/G snv 0.51 0.51 0.700 1.000 1 2010 2010