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: rs960709
rs960709
5 0.882 0.120 5 151081488 intron variant A/G;T snv 0.800 1.000 1 2013 2013
dbSNP: rs4958880
rs4958880
4 0.851 0.160 5 151058916 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs3792783
rs3792783
3 0.882 0.280 5 151076171 intron variant A/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs2233287
rs2233287
2 0.925 0.160 5 151060536 intron variant G/A snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs10036748
rs10036748
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.010 1.000 1 2012 2012