RFX7, regulatory factor X7, 64864

N. diseases: 13; N. variants: 6
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: rs16976734
rs16976734
0.925 0.120 15 56090097 3 prime UTR variant A/G snv 0.12
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.800 1.000 1 2014 2014
dbSNP: rs11638850
rs11638850
15 56141657 intron variant A/C snv 0.63
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs16976734
rs16976734
0.925 0.120 15 56090097 3 prime UTR variant A/G snv 0.12
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs2713933
rs2713933
15 56246364 intron variant C/A snv 0.30
RDW - Red blood cell distribution width result
0.700 1.000 1 2019 2019
dbSNP: rs2713933
rs2713933
15 56246364 intron variant C/A snv 0.30
Red cell distribution width determination
0.700 1.000 1 2019 2019
dbSNP: rs2713939
rs2713939
15 56202604 intron variant A/G snv 0.57
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs33984059
rs33984059
1.000 0.080 15 56093670 missense variant A/G snv 1.5E-02 1.3E-02
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
Neoplasms; Male Urogenital Diseases 0.700 1.000 1 2018 2018
dbSNP: rs8030605
rs8030605
15 56212400 intron variant G/A snv 0.12
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2018 2018