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: rs10065637
rs10065637
2 1.000 0.040 5 56143024 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs71624119
rs71624119
7 0.776 0.200 5 56144903 intron variant G/A snv 0.17 0.700 1.000 2 2015 2016
dbSNP: rs7731626
rs7731626
15 0.716 0.240 5 56148856 intron variant G/A snv 0.30 0.700 1.000 1 2015 2015