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: rs157580
rs157580
14 0.882 0.160 19 44892009 intron variant G/A snv 0.69 0.800 1.000 2 2012 2019
dbSNP: rs157582
rs157582
8 0.851 0.160 19 44892962 intron variant C/T snv 0.24 0.29 0.700 1.000 3 2016 2019
dbSNP: rs2075650
rs2075650
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.700 1.000 2 2012 2013
dbSNP: rs10119
rs10119
5 0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs157581
rs157581
3 0.925 0.080 19 44892457 synonymous variant T/C snv 0.25 0.29 0.700 1.000 1 2012 2012