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: rs693955
rs693955
2 0.925 0.040 6 44224183 intron variant A/C snv 0.85 0.010 1.000 1 2015 2015
dbSNP: rs747199
rs747199
2 0.925 0.040 6 44226608 intron variant G/C snv 0.15 0.010 1.000 1 2015 2015