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: rs4374383
rs4374383
10 0.776 0.200 2 112013193 intron variant A/G snv 0.58 0.710 1.000 2 2012 2018
dbSNP: rs6726639
rs6726639
1 1.000 0.080 2 111995520 intron variant A/C snv 0.62 0.010 1.000 1 2017 2017