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: rs10503253
rs10503253
2 0.851 0.040 8 4323322 intron variant C/A snv 0.18 0.850 0.889 1 2011 2017
dbSNP: rs10503256
rs10503256
1 1.000 0.040 8 4356657 intron variant A/G snv 0.57 0.800 1.000 2 2011 2012
dbSNP: rs17067182
rs17067182
1 1.000 0.040 8 3729296 intron variant G/A snv 0.20 0.700 1.000 1 2011 2011