Gene: PHEX ×
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: rs1556020485
rs1556020485
PHEX
1 1.000 0.200 X 22076480 splice region variant T/C snv 0.700 0
dbSNP: rs1556020752
rs1556020752
PHEX
1 1.000 0.200 X 22077506 missense variant T/C snv 0.700 0
dbSNP: rs1556020770
rs1556020770
PHEX
1 1.000 0.200 X 22077540 stop gained G/A snv 0.700 0
dbSNP: rs1556020798
rs1556020798
PHEX
1 1.000 0.200 X 22077582 frameshift variant GAGA/- delins 0.700 0
dbSNP: rs1556020818
rs1556020818
PHEX
1 1.000 0.200 X 22077630 synonymous variant A/G snv 0.700 0
dbSNP: rs1556023495
rs1556023495
PHEX
1 1.000 0.200 X 22090444 missense variant C/A snv 0.700 0
dbSNP: rs1556023503
rs1556023503
PHEX
1 1.000 0.200 X 22090469 frameshift variant A/- del 0.700 0
dbSNP: rs1556023505
rs1556023505
PHEX
1 1.000 0.200 X 22090472 missense variant T/C snv 0.700 0
dbSNP: rs1556023528
rs1556023528
PHEX
1 1.000 0.200 X 22090502 splice region variant G/A;C snv 0.700 0
dbSNP: rs1556024541
rs1556024541
PHEX
1 1.000 0.200 X 22094082 stop gained G/T snv 0.700 0
dbSNP: rs1556025314
rs1556025314
PHEX
1 1.000 0.200 X 22097039 splice donor variant G/T snv 0.700 0
dbSNP: rs1556025936
rs1556025936
PHEX
1 1.000 0.200 X 22099003 splice acceptor variant CAG/TCA mnv 0.700 0
dbSNP: rs1556025968
rs1556025968
PHEX
1 1.000 0.200 X 22099027 inframe deletion AAG/- delins 0.700 0
dbSNP: rs1556026027
rs1556026027
PHEX
1 1.000 0.200 X 22099094 missense variant T/A snv 0.700 0
dbSNP: rs1556026033
rs1556026033
PHEX
1 1.000 0.200 X 22099109 missense variant A/G snv 0.700 0
dbSNP: rs1556026042
rs1556026042
PHEX
1 1.000 0.200 X 22099114 frameshift variant A/- delins 0.700 0
dbSNP: rs1556029499
rs1556029499
PHEX
1 1.000 0.200 X 22111490 stop gained G/A snv 0.700 0
dbSNP: rs1556029516
rs1556029516
PHEX
1 1.000 0.200 X 22111520 frameshift variant T/- delins 0.700 0
dbSNP: rs1556029519
rs1556029519
PHEX
1 1.000 0.200 X 22111524 missense variant CA/AT mnv 0.700 0
dbSNP: rs1556030465
rs1556030465
PHEX
1 1.000 0.200 X 22114500 missense variant T/C snv 0.700 0
dbSNP: rs1556030487
rs1556030487
PHEX
1 1.000 0.200 X 22114553 frameshift variant A/- del 0.700 0
dbSNP: rs1556030502
rs1556030502
PHEX
1 1.000 0.200 X 22114581 stop gained G/T snv 0.700 0
dbSNP: rs1556036014
rs1556036014
PHEX
1 1.000 0.200 X 22133522 splice acceptor variant G/C snv 0.700 0
dbSNP: rs1556070724
rs1556070724
PHEX
1 1.000 0.200 X 22178271 splice acceptor variant A/G snv 0.700 0
dbSNP: rs1556070890
rs1556070890
PHEX
1 1.000 0.200 X 22178313 missense variant A/C snv 0.700 0