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: rs1432214488
rs1432214488
MCAM
1 1.000 0.080 11 119315209 missense variant C/G snv 0.010 1.000 1 2015 2015
dbSNP: rs375120544
rs375120544
RET
1 1.000 0.080 10 43105044 missense variant G/A;C snv 4.2E-06; 1.3E-05 0.010 1.000 1 2010 2010
dbSNP: rs774383499
rs774383499
PDLIM3
1 1.000 0.080 4 185502466 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.010 1.000 1 2015 2015