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: rs11676922
rs11676922
4 0.925 0.160 2 100190478 intron variant T/A snv 0.51 0.800 1.000 2 2010 2014
dbSNP: rs10209110
rs10209110
1 1.000 0.120 2 100056230 intron variant C/T snv 0.47 0.800 1.000 1 2012 2012
dbSNP: rs6712515
rs6712515
3 0.925 0.160 2 100190052 intron variant T/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs11123810
rs11123810
2 0.925 0.200 2 100142823 intron variant T/C snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs11123811
rs11123811
1 1.000 0.120 2 100143710 intron variant T/C snv 0.55 0.700 1.000 1 2015 2015