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: rs4894535
rs4894535
FNDC3B
1.000 0.040 3 172277815 intron variant C/A;T snv
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.800 1.000 1 2013 2013
dbSNP: rs9647379
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32
CUI: C0018810
Disease: heart rate
heart rate 		0.800 1.000 1 2013 2013
dbSNP: rs4535251
rs4535251
FNDC3B
3 172208583 intron variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2013 2013
dbSNP: rs6445055
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24
CUI: C0524957
Disease: Corneal Topography
Corneal Topography 		0.700 1.000 1 2013 2013
dbSNP: rs7652177
rs7652177
FNDC3B
3 172251287 missense variant C/G snv 0.54 0.61
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010