HBS1L, HBS1 like translational GTPase, 10767

N. diseases: 23; N. variants: 32
Disease: Red Blood Cell Count measurement ×
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: rs7775698
rs7775698 		1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 2 2009 2012
dbSNP: rs1547247
rs1547247 		6 135069698 intron variant G/A snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 1 2009 2019
dbSNP: rs9376090
rs9376090 		6 135090090 intron variant T/C snv 0.19
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.800 1.000 1 2009 2018
dbSNP: rs34164109
rs34164109 		6 135100038 intron variant C/T snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2017 2017
dbSNP: rs35367489
rs35367489 		6 135023317 intron variant G/A snv 0.32
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs41294858
rs41294858 		6 135091498 intron variant T/C snv 0.11
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs7776054
rs7776054 		6 135097778 intron variant A/G snv 0.24
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs9399135
rs9399135 		6 135047176 intron variant G/A snv 0.62
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2016 2016