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: rs387907219
rs387907219
TRPV4
1 1.000 0.080 12 109800659 missense variant C/G;T snv 1.6E-05 0.800 1.000 1 2011 2011
dbSNP: rs387907220
rs387907220
TRPV4
1 1.000 0.080 12 109800662 missense variant C/A snv 0.800 1.000 1 2011 2011
dbSNP: rs515726170
rs515726170
TRPV4
1 1.000 0.080 12 109800652 missense variant G/C snv 0.800 1.000 1 2011 2011
dbSNP: rs267607144
rs267607144
TRPV4
17 0.716 0.360 12 109800665 missense variant C/T snv 0.700 0