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: rs6897932
rs6897932
25 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 0.800 1.000 3 2011 2017
dbSNP: rs7717955
rs7717955
3 0.925 0.200 5 35862739 intron variant C/T snv 0.23 0.700 1.000 1 2011 2011