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: rs1408416
rs1408416
1 1 64148812 intron variant G/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs6671162
rs6671162
1 1 64159463 intron variant A/G snv 0.33 0.700 1.000 1 2018 2018