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: rs121912634
rs121912634
TRPV4
2 0.925 0.080 12 109798768 missense variant T/C snv 0.800 1.000 3 2009 2012
dbSNP: rs121912635
rs121912635
TRPV4
2 0.925 0.080 12 109788462 missense variant C/A snv 0.800 1.000 3 2009 2012
dbSNP: rs267607148
rs267607148
TRPV4
4 0.882 0.120 12 109800639 missense variant C/T snv 0.800 1.000 3 2009 2012
dbSNP: rs267607149
rs267607149
TRPV4
5 0.851 0.120 12 109784385 missense variant C/T snv 0.800 1.000 3 2009 2012
dbSNP: rs77975504
rs77975504
TRPV4
6 0.827 0.280 12 109792695 missense variant C/T snv 0.800 1.000 3 2009 2012
dbSNP: rs515726159
rs515726159
TRPV4
2 0.925 0.080 12 109792689 missense variant A/G snv 0.700 1.000 3 2009 2012
dbSNP: rs515726160
rs515726160
TRPV4
2 0.925 0.080 12 109792678 missense variant C/A snv 0.700 1.000 3 2009 2012
dbSNP: rs515726164
rs515726164
TRPV4
2 0.925 0.080 12 109792379 missense variant C/T snv 0.700 1.000 3 2009 2012
dbSNP: rs515726165
rs515726165
TRPV4
2 0.925 0.080 12 109786716 missense variant C/T snv 0.700 1.000 3 2009 2012
dbSNP: rs116571438
rs116571438
TRPV4
2 0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 0.700 0
dbSNP: rs267607144
rs267607144
TRPV4
17 0.716 0.360 12 109800665 missense variant C/T snv 0.700 0