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: rs117565673
rs117565673
16 88977046 5 prime UTR variant T/C snv 3.7E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2016 2019
dbSNP: rs12102677
rs12102677
16 88950086 intron variant A/C snv 0.34
Platelet mean volume determination (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs475796
rs475796
0.925 0.040 16 88904368 intron variant C/G;T snv
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 1.000 1 2018 2018
dbSNP: rs475796
rs475796
0.925 0.040 16 88904368 intron variant C/G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis
Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs7188793
rs7188793
1.000 0.040 16 88976453 intron variant A/G snv 0.69
CUI: C0042900
Disease: Vitiligo
Vitiligo
Skin and Connective Tissue Diseases 0.700 1.000 1 2016 2016
dbSNP: rs553618592
rs553618592
1.000 0.080 16 88879331 missense variant G/A snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs745972870
rs745972870
1.000 0.080 16 88885246 missense variant C/T snv 2.4E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs774310781
rs774310781
1.000 0.080 16 88879380 missense variant C/T snv 4.8E-05 4.2E-05
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
Digestive System Diseases; Neoplasms 0.700 0
dbSNP: rs13333659
rs13333659
1.000 0.040 16 88972472 intron variant G/T snv 0.13
CUI: C0338656
Disease: Impaired cognition
Impaired cognition
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs13333659
rs13333659
1.000 0.040 16 88972472 intron variant G/T snv 0.13
CUI: C0234985
Disease: Mental deterioration
Mental deterioration
Mental Disorders 0.010 1.000 1 2019 2019