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: rs267607194
rs267607194
1 1.000 16 75640258 missense variant A/T snv 0.800 1.000 1 2010 2010
dbSNP: rs146955132
rs146955132
1 1.000 16 75634266 missense variant G/C snv 3.6E-04 2.2E-04 0.700 0
dbSNP: rs587776688
rs587776688
1 1.000 16 75636504 frameshift variant -/AA delins 0.700 0