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: rs2799573
rs2799573
5 0.851 0.040 10 18312999 intron variant T/C snv 0.20 0.700 1.000 1 2013 2013
dbSNP: rs7893279
rs7893279
2 1.000 0.040 10 18456176 intron variant T/G snv 0.10 0.700 1.000 1 2017 2017