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: rs35311343
rs35311343
1 1.000 0.040 4 186082575 missense variant C/G snv 1.5E-03 1.6E-03 0.010 1.000 1 2017 2017
dbSNP: rs753482575
rs753482575
1 1.000 0.040 4 186078995 missense variant A/T snv 8.0E-06 2.8E-05 0.010 1.000 1 2017 2017