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: rs798502
rs798502
4 1.000 0.040 7 2750246 intron variant A/C;G snv 0.800 1.000 3 2011 2017
dbSNP: rs1182188
rs1182188
8 0.827 0.120 7 2830351 intron variant T/C snv 0.26 0.700 1.000 2 2015 2016