WNT2, Wnt family member 2, 7472

N. diseases: 96; N. variants: 9
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: rs4730775
rs4730775
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41
CUI: C4082974
Disease: Dupuytren's Disease
Dupuytren's Disease
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.710 0.500 2 2011 2012
dbSNP: rs39312
rs39312
7 117314731 intron variant A/C snv 0.43
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 2 2018 2019
dbSNP: rs114167782
rs114167782
7 117299233 intron variant C/T snv 3.0E-02
CUI: C0037369
Disease: Smoking
Smoking
Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs114167782
rs114167782
7 117299233 intron variant C/T snv 3.0E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors
Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs4730775
rs4730775
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41
CUI: C0013312
Disease: Dupuytren Contracture
Dupuytren Contracture
Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2011 2011
dbSNP: rs2896218
rs2896218
0.925 0.040 7 117279924 intron variant G/A snv 0.60
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs2896218
rs2896218
0.925 0.040 7 117279924 intron variant G/A snv 0.60
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs3729629
rs3729629
1.000 0.040 7 117286578 intron variant C/G;T snv 0.50
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs3779547
rs3779547
1.000 0.040 7 117290908 intron variant A/G;T snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs39315
rs39315
1.000 0.080 7 117323508 intron variant T/C;G snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs39315
rs39315
1.000 0.080 7 117323508 intron variant T/C;G snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2016 2016
dbSNP: rs4727847
rs4727847
1.000 0.040 7 117288317 intron variant T/C;G snv
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs4730775
rs4730775
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41
CUI: C0030848
Disease: Peyronie Disease
Peyronie Disease
Skin and Connective Tissue Diseases; Male Urogenital Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs4730775
rs4730775
0.851 0.200 7 117277064 3 prime UTR variant C/T snv 0.41
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs6950765
rs6950765
0.925 0.040 7 117281176 intron variant C/G snv 0.64
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs6950765
rs6950765
0.925 0.040 7 117281176 intron variant C/G snv 0.64
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
Mental Disorders 0.010 1.000 1 2011 2011