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: rs10793962
rs10793962
ABO
9 133253728 non coding transcript exon variant A/T snv 0.11
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2018 2018
dbSNP: rs8176741
rs8176741
ABO
9 133256074 synonymous variant G/A snv 0.12 0.11
CUI: C0040420
Disease: Tonometry
Tonometry 		0.700 1.000 2 2017 2018
dbSNP: rs10793962
rs10793962
ABO
9 133253728 non coding transcript exon variant A/T snv 0.11
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2019 2019
dbSNP: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10901252
rs10901252
ABO
9 133252613 non coding transcript exon variant G/C snv 0.11
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs115478735
rs115478735
ABO
9 133274295 intron variant A/T snv 0.14
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs116552240
rs116552240
ABO
9 133273682 intron variant A/T snv
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.700 1.000 1 2015 2015
dbSNP: rs12216891
rs12216891
ABO
9 133251979 non coding transcript exon variant C/T snv 7.8E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2018 2018
dbSNP: rs139840563
rs139840563
ABO
9 133271018 intron variant -/GACAA;GACAAGACAA delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs149037075
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs149037075
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs149037075
rs149037075
ABO
9 133255469 3 prime UTR variant CTGT/- delins 0.15
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs187099314
rs187099314
ABO
9 133255354 3 prime UTR variant C/G;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs202001822
rs202001822
ABO
9 133270005 intron variant A/-;AA;AAA;AAAAAA delins
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2019 2019
dbSNP: rs2769071
rs2769071
ABO
9 133270565 intron variant G/A snv
CUI: C3272931
Disease: Fibroblast Growth Factor 23 Measurement
Fibroblast Growth Factor 23 Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs35230453
rs35230453
ABO
9 133266030 intron variant AA/-;A;AAA;AAAA;AAAAA;AAAAAA;AAAAAAAAAAA delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs491626
rs491626
ABO
9 133269461 intron variant T/A;C snv
CUI: C0201973
Disease: Creatine kinase measurement
Creatine kinase measurement 		0.700 1.000 1 2018 2018
dbSNP: rs492488
rs492488
ABO
9 133269548 intron variant A/C;G;T snv
CUI: C0523677
Disease: Glycine measurement
Glycine measurement 		0.700 1.000 1 2019 2019
dbSNP: rs492488
rs492488
ABO
9 133269548 intron variant A/C;G;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs582094
rs582094
ABO
9 133270074 intron variant T/A snv
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		0.700 1.000 1 2018 2018
dbSNP: rs587611953
rs587611953
ABO
9 133270004 intron variant C/A snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs587729126
rs587729126
ABO
9 133263363 intron variant CACCACTACGCC/- delins
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs612169
rs612169
ABO
9 133268030 intron variant G/A snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.800 1.000 1 2013 2017
dbSNP: rs62641786
rs62641786
ABO
9 133255290 3 prime UTR variant T/C;G snv
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test) 		0.700 1.000 1 2019 2019