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: rs3743347
rs3743347
IQCH ; AAGAB
15 67254963 intron variant C/A;T snv 0.26; 8.2E-06
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7173826
rs7173826
AAGAB
15 67236036 missense variant T/C;G snv 8.0E-06; 0.37
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.700 1.000 1 2019 2019