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: rs700518
rs700518
13 0.732 0.320 15 51236915 synonymous variant T/C snv 0.43 0.40 0.010 1.000 1 2013 2013
dbSNP: rs749292
rs749292
4 0.851 0.160 15 51266534 intron variant G/A snv 0.44 0.010 1.000 1 2019 2019