rs56848936, SYMPK

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.710 1.000 1 2017 2017
Adenocarcinoma of large intestine
CUI: C1319315
Disease: Adenocarcinoma of large intestine
432 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
Colonic Neoplasms
CUI: C0009375
Disease: Colonic Neoplasms
45 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
CUI: C1837315
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
374 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
CUI: C2675481
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
370 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
CUI: C3554460
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
373 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
CUI: C2677123
Disease: COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
368 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
Colorectal Neoplasms
CUI: C0009404
Disease: Colorectal Neoplasms
609 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
Malignant neoplasm of large intestine
CUI: C0346629
Disease: Malignant neoplasm of large intestine
375 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.700 1.000 1 2017 2017
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 0.010 1.000 1 2017 2017