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: rs7946012
rs7946012
11 2571301 intron variant C/T snv 1.1E-02 4.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs79972789
rs79972789
11 2803343 intron variant C/G;T snv 1.8E-02
CUI: C1629609
Disease: Age at menopause
Age at menopause
0.700 1.000 1 2013 2013