Gene: TRPV4 ×
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: rs116571438
rs116571438
TRPV4
2 0.925 0.080 12 109788483 missense variant G/A;T snv 8.0E-06 0.700 0
dbSNP: rs121912632
rs121912632
TRPV4
3 0.882 0.080 12 109792407 missense variant C/T snv 0.700 0
dbSNP: rs121912633
rs121912633
TRPV4
10 0.790 0.240 12 109792396 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs121912634
rs121912634
TRPV4
2 0.925 0.080 12 109798768 missense variant T/C snv 0.700 0
dbSNP: rs121912635
rs121912635
TRPV4
2 0.925 0.080 12 109788462 missense variant C/A snv 0.700 0
dbSNP: rs121912636
rs121912636
TRPV4
2 0.925 0.120 12 109798775 missense variant T/A;C snv 4.0E-06 0.700 0
dbSNP: rs121912637
rs121912637
TRPV4
5 0.851 0.160 12 109784378 missense variant G/A;C snv 0.700 0
dbSNP: rs267607147
rs267607147
TRPV4
2 0.925 0.120 12 109784379 missense variant G/A;C snv 0.700 0
dbSNP: rs267607148
rs267607148
TRPV4
4 0.882 0.120 12 109800639 missense variant C/T snv 0.700 0
dbSNP: rs267607149
rs267607149
TRPV4
5 0.851 0.120 12 109784385 missense variant C/T snv 0.700 0
dbSNP: rs267607150
rs267607150
TRPV4
2 0.925 0.080 12 109792671 missense variant T/C snv 0.700 0
dbSNP: rs387906324
rs387906324
TRPV4
2 0.925 0.080 12 109808308 missense variant C/T snv 0.700 0
dbSNP: rs387906902
rs387906902
TRPV4
3 0.925 0.080 12 109793560 missense variant G/C;T snv 4.0E-06 0.700 0
dbSNP: rs387906903
rs387906903
TRPV4
2 0.925 0.120 12 109803113 missense variant T/C snv 0.700 0
dbSNP: rs387906904
rs387906904
TRPV4
5 0.851 0.080 12 109803009 missense variant G/A snv 0.700 0
dbSNP: rs387906906
rs387906906
TRPV4
3 0.925 0.120 12 109786827 missense variant G/A snv 0.700 0
dbSNP: rs387906907
rs387906907
TRPV4
3 0.925 0.120 12 109800645 missense variant T/C snv 0.700 0
dbSNP: rs397514473
rs397514473
TRPV4
2 0.925 0.120 12 109814531 missense variant G/A snv 0.700 0
dbSNP: rs397514474
rs397514474
TRPV4
3 0.925 0.120 12 109814565 missense variant C/A snv 0.700 0
dbSNP: rs515726152
rs515726152
TRPV4
2 0.925 0.120 12 109798742 missense variant C/A snv 0.700 0
dbSNP: rs515726153
rs515726153
TRPV4
1 1.000 0.040 12 109796638 missense variant T/C snv 0.700 0
dbSNP: rs515726154
rs515726154
TRPV4
1 1.000 0.040 12 109794406 inframe deletion AAG/- delins 0.700 0
dbSNP: rs515726155
rs515726155
TRPV4
1 1.000 0.040 12 109793945 inframe insertion -/GGA delins 0.700 0
dbSNP: rs515726157
rs515726157
TRPV4
2 1.000 0.040 12 109792704 missense variant T/C snv 0.700 0
dbSNP: rs515726158
rs515726158
TRPV4
2 0.925 0.120 12 109792702 missense variant A/G snv 0.700 0