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: rs782627671
rs782627671
2 1.000 0.040 19 41869159 missense variant C/T snv 4.0E-06 0.010 1.000 1 2018 2018