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: rs7204230
rs7204230
3 16 53158419 intron variant T/C snv 0.31 0.800 1.000 1 2013 2013
dbSNP: rs11859517
rs11859517
1 16 53147335 intron variant C/T snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs12598049
rs12598049
1 16 53282942 intron variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs6499550
rs6499550
1 16 53308542 intron variant C/T snv 0.31 0.700 1.000 1 2017 2017