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: rs10891343
rs10891343
2 11 112209661 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs2250417
rs2250417
5 1.000 0.080 11 112214593 intron variant T/C snv 0.44 0.700 1.000 1 2014 2014
dbSNP: rs7131094
rs7131094
1 11 112174194 intron variant C/T snv 0.17 0.700 1.000 1 2014 2014