Source: ALL

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: rs11920918
rs11920918
UBXN7
3 196368689 intron variant G/A snv 8.5E-03
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11920918
rs11920918
UBXN7
3 196368689 intron variant G/A snv 8.5E-03
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs11920918
rs11920918
UBXN7
3 196368689 intron variant G/A snv 8.5E-03
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs150895667
rs150895667
UBXN7 ; UBXN7-AS1
3 196430801 intron variant A/G snv 2.4E-03
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2018 2018
dbSNP: rs34801745
rs34801745
UBXN7
3 196388626 intron variant G/C snv 0.36
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs6583310
rs6583310
UBXN7
3 196444114 regulatory region variant G/C snv 0.54
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs9860931
rs9860931
UBXN7
3 196369580 intron variant C/A;T snv
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019