Source: GWASCAT

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: rs1553318
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 2 2015 2018
dbSNP: rs1553318
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs1553318
rs1553318
HAVCR1
5 157052312 intron variant G/A;C snv 6.2E-03; 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 2 2015 2018
dbSNP: rs10066168
rs10066168
HAVCR1
5 157057207 intron variant C/G;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2019 2019
dbSNP: rs10066168
rs10066168
HAVCR1
5 157057207 intron variant C/G;T snv
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.700 1.000 1 2019 2019
dbSNP: rs17573010
rs17573010
HAVCR1
5 157050820 intron variant G/A snv 3.0E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6878069
rs6878069
HAVCR1
5 157044058 intron variant A/G snv 0.50
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs6889164
rs6889164
HAVCR1
5 157039767 intron variant T/C snv 0.28
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs870581
rs870581
HAVCR1
5 157055658 intron variant G/A snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018