Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.020 0.500 2 2004 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0005695
Disease: Bladder Neoplasm
Bladder Neoplasm
0.020 0.500 2 2004 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
Malignant neoplasm of urinary bladder
0.020 0.500 2 2004 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2014 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension
0.010 1.000 1 2010 2010
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0013384
Disease: Dyskinetic syndrome
Dyskinetic syndrome
0.010 1.000 1 2010 2010
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0280324
Disease: Laryngeal Squamous Cell Carcinoma
Laryngeal Squamous Cell Carcinoma
0.010 1.000 1 2016 2016
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.010 < 0.001 1 2004 2004
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2010 2010
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0243026
Disease: Sepsis
Sepsis
0.010 1.000 1 2015 2015
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0040425
Disease: Tonsillitis
Tonsillitis
0.010 1.000 1 2012 2012
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
0.010 1.000 1 2016 2016
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia
0.010 < 0.001 1 2014 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.010 < 0.001 1 2004 2004
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.010 1.000 1 2016 2016
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2010 2010
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 < 0.001 1 2014 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2014 2014
dbSNP: rs1043210477
rs1043210477
0.701 0.520 3 49358250 missense variant G/A snv
CUI: C0036690
Disease: Septicemia
Septicemia
0.010 1.000 1 2015 2015