Source: GWASDB

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: rs12493607
rs12493607
0.882 0.080 3 30641447 intron variant G/C;T snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.710 1.000 1 2013 2014
dbSNP: rs10212320
rs10212320
3 30632373 non coding transcript exon variant C/T snv 7.2E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs10212320
rs10212320
3 30632373 non coding transcript exon variant C/T snv 7.2E-03
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs3773643
rs3773643
3 30668751 intron variant A/G snv 0.19
CUI: C0040420
Disease: Tonometry
Tonometry
0.700 1.000 1 2007 2007
dbSNP: rs9838771
rs9838771
3 30657290 intron variant G/A snv 2.5E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs9838771
rs9838771
3 30657290 intron variant G/A snv 2.5E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs9838771
rs9838771
3 30657290 intron variant G/A snv 2.5E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012