Source: ALL
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: rs193922391
rs193922391
MYL3
1 1.000 0.080 3 46858413 missense variant T/C snv 5.6E-05 2.8E-05 0.700 1.000 4 1996 2013