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: rs1384270958
rs1384270958
1 1.000 0.040 10 121500883 missense variant C/G snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1554927408
rs1554927408
12 0.742 0.480 10 121515254 missense variant C/T snv 0.010 1.000 1 2017 2017