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: rs16942341
rs16942341
15 88845674 synonymous variant C/T snv 3.8E-02 6.4E-02
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2010 2011
dbSNP: rs2280470
rs2280470
15 88852395 intron variant A/G snv 0.68
CUI: C0489786
Disease: Height
Height
0.700 1.000 2 2010 2013
dbSNP: rs11854545
rs11854545
15 88825873 intron variant G/A;T snv
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs11854545
rs11854545
15 88825873 intron variant G/A;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs16942333
rs16942333
15 88845033 intron variant A/G snv 3.3E-02
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs2351491
rs2351491
15 88854874 synonymous variant C/T snv 0.50 0.48
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011
dbSNP: rs8026235
rs8026235
15 88806225 intron variant A/C snv 1.7E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs8041863
rs8041863
15 88816458 intron variant T/A;G snv
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2008 2008
dbSNP: rs938609
rs938609
15 88855400 missense variant T/A snv 0.51 0.52
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011