HBS1L, HBS1 like translational GTPase, 10767

N. diseases: 23; N. variants: 32
Disease: Eosinophil count procedure ×
Source: GWASCAT ×
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9373124
rs9373124 		6 135102071 intron variant T/C snv 0.33
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.800 1.000 1 2011 2011
dbSNP: rs2210366
rs2210366 		6 135094070 intron variant G/A snv 0.34
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2018 2018
dbSNP: rs34208856
rs34208856 		6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs35959442
rs35959442 		6 135103041 5 prime UTR variant C/G;T snv 0.24
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs56131511
rs56131511 		6 135068381 intron variant G/A;C snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs9402682
rs9402682 		6 135085045 intron variant G/T snv 0.42
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016