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: rs10183486
rs10183486
1 2 171134461 intron variant C/T snv 0.41 0.800 1.000 1 2012 2012
dbSNP: rs930036
rs930036
1 2 171084508 intron variant G/A snv 0.47 0.700 1.000 1 2015 2015