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: rs6812849
rs6812849
1 1.000 0.040 4 165951384 intron variant C/A;T snv 0.800 1.000 1 2013 2013
dbSNP: rs7691872
rs7691872
1 1.000 0.040 4 165944433 intron variant G/C;T snv 0.700 1.000 1 2013 2013