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: rs6464214
rs6464214
2 0.925 0.120 7 139754366 intron variant A/G snv 0.37 0.010 1.000 1 2018 2018
dbSNP: rs7456421
rs7456421
4 0.882 0.120 7 139715976 synonymous variant G/C snv 0.27 0.37 0.010 1.000 1 2018 2018