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: rs11014166
rs11014166
10 0.882 0.040 10 18419869 intron variant A/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs12258967
rs12258967
5 10 18439030 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17613287
rs17613287
4 10 18430748 intron variant A/T snv 0.27 0.700 1.000 1 2018 2018