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: rs10036748
rs10036748
11 0.752 0.360 5 151078585 intron variant C/A;T snv 0.830 1.000 6 2009 2017
dbSNP: rs7708392
rs7708392
13 0.732 0.400 5 151077924 intron variant G/C snv 0.44 0.730 1.000 6 2009 2018
dbSNP: rs6889239
rs6889239
1 1.000 0.080 5 151078210 intron variant T/C snv 0.41 0.700 1.000 2 2015 2016
dbSNP: rs4958880
rs4958880
4 0.851 0.160 5 151058916 intron variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs960709
rs960709
5 0.882 0.120 5 151081488 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4958881
rs4958881
7 0.827 0.280 5 151070675 intron variant T/C snv 0.21 0.010 1.000 1 2013 2013