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: rs149544854
rs149544854
2 1.000 0.040 6 31755003 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs707939
rs707939
5 0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 0.700 1.000 1 2017 2017