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: rs10262453
rs10262453
BBS9
0.925 0.080 7 33216427 intron variant A/C snv 0.27
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		0.700 1.000 1 2012 2012
dbSNP: rs1421344
rs1421344
BBS9
1.000 0.080 7 33844140 intron variant G/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs17786463
rs17786463
BBS9
7 33393339 intron variant A/C;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs2109525
rs2109525
BBS9
7 33371655 intron variant T/G snv 0.12
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2013 2013
dbSNP: rs6948754
rs6948754
BBS9
7 33804209 intron variant T/C snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011