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: rs2713936
rs2713936
TEX9
15 56253787 intron variant A/C snv 0.32
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs12908766
rs12908766
MNS1 ; TEX9
15 56423932 intron variant G/A snv 0.75
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs144803255
rs144803255
TEX9
1.000 0.040 15 56403547 intron variant G/A;C snv
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		0.700 1.000 1 2014 2014
dbSNP: rs2713933
rs2713933
RFX7 ; TEX9
15 56246364 intron variant C/A snv 0.30
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs2713933
rs2713933
RFX7 ; TEX9
15 56246364 intron variant C/A snv 0.30
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs2713936
rs2713936
TEX9
15 56253787 intron variant A/C snv 0.32
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs35812910
rs35812910
MNS1 ; TEX9
15 56439447 intron variant AAAAAA/-;AAAA;AAAAA;AAAAAAA delins
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2019 2019
dbSNP: rs35812910
rs35812910
MNS1 ; TEX9
15 56439447 intron variant AAAAAA/-;AAAA;AAAAA;AAAAAAA delins
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs71297631
rs71297631
TEX9
15 56369974 intron variant -/A ins
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2017 2017
dbSNP: rs71297631
rs71297631
TEX9
15 56369974 intron variant -/A ins
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2017 2017
dbSNP: rs7168886
rs7168886
TEX9
15 56332184 intron variant G/A snv
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs7168886
rs7168886
TEX9
15 56332184 intron variant G/A snv
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016