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: rs2764261
rs2764261
3 6 108606639 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3800229
rs3800229
4 1.000 0.040 6 108675760 intron variant G/T snv 0.54 0.700 1.000 1 2017 2017