Gene: PKHD1 ×
Source: GWASCAT ×
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: rs11754532
rs11754532
PKHD1
1 1.000 0.040 6 51786884 intron variant C/G snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs1326570
rs1326570
PKHD1
1 1.000 0.040 6 51800799 intron variant T/A;C snv 0.75 0.700 1.000 1 2017 2017
dbSNP: rs2104521
rs2104521
PKHD1
1 1.000 0.040 6 51791701 intron variant T/C snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs2104522
rs2104522
PKHD1
1 1.000 0.040 6 51791753 intron variant G/A snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs2397061
rs2397061
PKHD1
1 1.000 0.040 6 51774079 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs2894788
rs2894788
PKHD1
1 1.000 0.040 6 51778470 intron variant C/T snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs41412044
rs41412044
PKHD1
1 1.000 0.040 6 51773363 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs4715233
rs4715233
PKHD1
1 1.000 0.040 6 51791590 intron variant A/G snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs6458777
rs6458777
PKHD1
1 1.000 0.040 6 51790609 intron variant A/G snv 0.58 0.700 1.000 1 2017 2017
dbSNP: rs6922497
rs6922497
PKHD1
1 1.000 0.040 6 51772913 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs6940892
rs6940892
PKHD1
1 1.000 0.040 6 51789633 intron variant T/C snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs728996
rs728996
PKHD1
1 1.000 0.040 6 51778216 intron variant C/T snv 0.56 0.700 1.000 1 2017 2017
dbSNP: rs9370050
rs9370050
PKHD1
1 1.000 0.040 6 51755123 intron variant T/C snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs9474070
rs9474070
PKHD1
1 1.000 0.040 6 51783015 intron variant G/A snv 0.75 0.700 1.000 1 2017 2017