rs1559279177, HJV

N. diseases: 5
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.
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.851 0.160 1 146018661 frameshift variant G/- del 0.700 0
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.851 0.160 1 146018661 frameshift variant G/- del 0.700 0
HEMOCHROMATOSIS, TYPE 2A
CUI: C1865614
Disease: HEMOCHROMATOSIS, TYPE 2A
13 0.851 0.160 1 146018661 frameshift variant G/- del 0.700 0
Hypogonadism
CUI: C0020619
Disease: Hypogonadism
24 0.851 0.160 1 146018661 frameshift variant G/- del 0.700 0
Secondary hypothyroidism
CUI: C3665349
Disease: Secondary hypothyroidism
2 0.851 0.160 1 146018661 frameshift variant G/- del 0.700 0