Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs122458138
rs122458138
ACSL4
1.000 0.080 X 109661643 missense variant G/T snv
CUI: C1845672
Disease: Mental Retardation, X-Linked 63
Mental Retardation, X-Linked 63 		0.800 1.000 1 2002 2002
dbSNP: rs122458139
rs122458139
ACSL4
1.000 0.080 X 109674403 missense variant G/A snv
CUI: C1845672
Disease: Mental Retardation, X-Linked 63
Mental Retardation, X-Linked 63 		0.700 0
dbSNP: rs1569423317
rs1569423317
ACSL4
1.000 0.080 X 109669175 splice acceptor variant T/C snv
CUI: C1845672
Disease: Mental Retardation, X-Linked 63
Mental Retardation, X-Linked 63 		0.700 0
dbSNP: rs753267653
rs753267653
ACSL4
1.000 0.080 X 109682851 missense variant G/A snv 2.7E-05 9.5E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.700 0
dbSNP: rs1324805
rs1324805
ACSL4
1.000 0.040 X 109719433 intron variant A/G snv 0.45
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.010 1.000 1 2009 2009
dbSNP: rs1364685385
rs1364685385
ACSL4 ; KCNE5
1.000 0.080 X 109624828 missense variant G/A snv 9.3E-06
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.010 1.000 1 2019 2019