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: rs3786897
rs3786897
5 1.000 0.080 19 33402102 intron variant A/G snv 0.45 0.820 0.667 1 2011 2019
dbSNP: rs10406327
rs10406327
2 1.000 0.080 19 33399932 intron variant C/G;T snv 0.700 1.000 1 2019 2019