Source: GWASCAT

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: rs7775698
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2010 2010
dbSNP: rs9373124
rs9373124
HBS1L
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: rs7775698
rs7775698
HBS1L
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: rs7775698
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.800 1.000 1 2010 2012
dbSNP: rs7775698
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 1.000 1 2010 2012
dbSNP: rs9373124
rs9373124
HBS1L
6 135102071 intron variant T/C snv 0.33
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.800 1.000 1 2009 2012
dbSNP: rs7775698
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.800 1.000 4 2009 2013
dbSNP: rs7775698
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.800 1.000 3 2009 2013
dbSNP: rs7745098
rs7745098
HBS1L
1.000 0.120 6 135093866 intron variant C/G;T snv
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		0.800 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.800 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0474543
Disease: Hemoglobin A2 measurement
Hemoglobin A2 measurement 		0.700 1.000 1 2013 2013
dbSNP: rs9399137
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.800 1.000 2 2007 2015
dbSNP: rs7776054
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24
CUI: C0474543
Disease: Hemoglobin A2 measurement
Hemoglobin A2 measurement 		0.700 1.000 1 2015 2015
dbSNP: rs7776054
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2015 2015
dbSNP: rs9399137
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2015 2015
dbSNP: rs1331308
rs1331308
HBS1L
6 135083984 intron variant A/C snv 0.61
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs2210366
rs2210366
HBS1L
6 135094070 intron variant G/A snv 0.34
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs34164109
rs34164109
HBS1L
6 135100038 intron variant C/T snv 0.22
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs34208856
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs34208856
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016
dbSNP: rs34208856
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs34208856
rs34208856
HBS1L
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: rs34208856
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs35959442
rs35959442
HBS1L
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: rs41294858
rs41294858
HBS1L
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