APOC1, apolipoprotein C1, 341

N. diseases: 95; N. variants: 19
Disease: Alzheimer's Disease ×
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: rs4420638
rs4420638 		0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.820 1.000 11 2007 2019
dbSNP: rs56131196
rs56131196 		0.925 0.160 19 44919589 downstream gene variant G/A snv 0.18
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.710 1.000 4 2014 2019
dbSNP: rs483082
rs483082 		1.000 0.080 19 44912921 non coding transcript exon variant G/T snv 0.28
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 2 2017 2019
dbSNP: rs3925681
rs3925681 		1.000 0.080 19 44917843 intron variant G/A snv 0.36
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs584007
rs584007 		1.000 0.080 19 44913221 non coding transcript exon variant A/G snv 0.68
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs59325138
rs59325138 		1.000 0.080 19 44913034 non coding transcript exon variant C/G;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs11568822
rs11568822 		1.000 0.080 19 44914381 5 prime UTR variant -/CGTT delins
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.020 1.000 2 2014 2019
dbSNP: rs73052335
rs73052335 		1.000 0.080 19 44916825 intron variant A/C snv 8.6E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2018 2018