PRRX1, paired related homeobox 1, 5396

N. diseases: 134; N. variants: 11
Disease: Atrial Fibrillation ×
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: rs12142379
rs12142379 		1.000 0.080 1 170724397 intron variant T/C snv 4.7E-02
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs503706
rs503706 		1.000 0.080 1 170665943 intron variant T/C snv 0.63
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs520525
rs520525 		1.000 0.080 1 170669192 non coding transcript exon variant A/C;G snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2017 2017
dbSNP: rs593479
rs593479 		1.000 0.080 1 170673758 intron variant T/C snv 0.60
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2017 2017