MED7, mediator complex subunit 7, 9443

N. diseases: 8; N. variants: 2
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: rs13360007
rs13360007 		1.000 0.040 5 157150709 intron variant A/G snv 0.15
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs246871
rs246871 		0.882 0.160 5 157158243 intron variant T/C snv 0.42
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2014 2019
dbSNP: rs246871
rs246871 		0.882 0.160 5 157158243 intron variant T/C snv 0.42
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs246871
rs246871 		0.882 0.160 5 157158243 intron variant T/C snv 0.42
CUI: C1512409
Disease: Hepatocarcinogenesis
Hepatocarcinogenesis 		Pathological Conditions, Signs and Symptoms; Neoplasms 0.010 1.000 1 2019 2019