PHF3, PHD finger protein 3, 23469

N. diseases: 12; N. variants: 28
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137853190
rs137853190
0.925 0.080 6 63720626 stop gained A/T snv 1.6E-05
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 1.000 2 2008 2010
dbSNP: rs137853190
rs137853190
0.925 0.080 6 63720626 stop gained A/T snv 1.6E-05
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs319924
rs319924
0.925 0.040 6 63777354 intron variant A/G;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs319924
rs319924
0.925 0.040 6 63777354 intron variant A/G;T snv
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs527236076
rs527236076
1.000 0.080 6 63762520 stop gained A/T snv 1.3E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.710 1.000 1 2019 2019
dbSNP: rs764229134
rs764229134
0.925 0.080 6 63726596 frameshift variant GT/- delins
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 1.000 1 2010 2010
dbSNP: rs869312188
rs869312188
6 63720752 frameshift variant -/CC delins
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs1168101857
rs1168101857
0.925 0.080 6 63726584 frameshift variant T/- del 1.3E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1168101857
rs1168101857
0.925 0.080 6 63726584 frameshift variant T/- del 1.3E-05
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1427770112
rs1427770112
1.000 0.080 6 63720949 frameshift variant TTCT/- delins
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1554163919
rs1554163919
1.000 0.080 6 63721235 frameshift variant ATTG/- delins
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1554163929
rs1554163929
1.000 0.080 6 63721353 frameshift variant T/- delins
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs527236064
rs527236064
1.000 0.080 6 63778111 missense variant C/T snv
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs527236070
rs527236070
1.000 0.080 6 63721651 frameshift variant -/TGCA delins
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs764229134
rs764229134
0.925 0.080 6 63726596 frameshift variant GT/- delins
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs776526721
rs776526721
1.000 0.080 6 63721201 frameshift variant C/- delins 3.2E-05
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs527236066
rs527236066
0.925 0.080 6 63762613 stop gained C/T snv 2.6E-05 7.0E-06
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs527236066
rs527236066
0.925 0.080 6 63762613 stop gained C/T snv 2.6E-05 7.0E-06
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs1415160006
rs1415160006
1.000 0.080 6 63720689 missense variant A/T snv 7.0E-06
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2019 2019
dbSNP: rs373203896
rs373203896
1.000 0.080 6 63721252 missense variant A/G snv 3.8E-05 1.4E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 1.000 1 2019 2019
dbSNP: rs1349879153
rs1349879153
1.000 0.080 6 63721795 missense variant C/A snv 2.7E-05 1.4E-05
Autosomal recessive retinitis pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.010 1.000 1 2010 2010
dbSNP: rs1165454778
rs1165454778
1.000 0.080 6 63720864 frameshift variant TA/- delins 1.4E-05
CUI: C1864446
Disease: Retinitis Pigmentosa 25
Retinitis Pigmentosa 25
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 0
dbSNP: rs527236067
rs527236067
1.000 0.080 6 63721226 stop gained G/T snv 3.2E-05 2.1E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.710 1.000 1 2012 2012
dbSNP: rs1435861529
rs1435861529
6 63762538 missense variant C/T snv 2.1E-05
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
Eye Diseases 0.700 0
dbSNP: rs779983752
rs779983752
1.000 0.080 6 63726641 stop gained A/C snv 3.9E-05 2.8E-05
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases 0.700 1.000 1 2018 2018