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: rs45544633
rs45544633
4 1.000 0.080 14 23417174 missense variant G/A snv 0.700 0
dbSNP: rs1343372308
rs1343372308
2 14 23413792 missense variant C/G snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs371855540
rs371855540
2 14 23415095 missense variant C/T snv 2.0E-05 3.5E-05 0.010 1.000 1 2016 2016