ASIC2, acid sensing ion channel subunit 2, 40

N. diseases: 2; N. variants: 21
Source: CURATED ×
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: rs11652874
rs11652874 		17 33643464 intron variant C/G snv 4.4E-02
CUI: C0017565
Disease: Gingival Hemorrhage
Gingival Hemorrhage 		Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs117364231
rs117364231 		17 33979404 intron variant C/T snv 1.7E-02
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2013 2013
dbSNP: rs12450841
rs12450841 		17 33323205 intron variant A/G snv 0.23
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17183972
rs17183972 		1.000 0.040 17 33094588 intron variant T/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17782805
rs17782805 		17 33568429 intron variant A/G snv 3.9E-02
CUI: C3893645
Disease: response to ACE inhibitor
response to ACE inhibitor 		0.700 1.000 1 2017 2017
dbSNP: rs2089164
rs2089164 		0.925 0.040 17 33384425 intron variant C/A;G;T snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2089164
rs2089164 		0.925 0.040 17 33384425 intron variant C/A;G;T snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs34187563
rs34187563 		1.000 0.040 17 33399144 intron variant G/C;T snv
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs35578035
rs35578035 		17 33422168 intron variant T/C snv 0.53
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs3925478
rs3925478 		1.000 0.040 17 33095784 intron variant C/G snv 0.71
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs3930349
rs3930349 		17 33148527 intron variant C/A snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4072512
rs4072512 		1.000 0.040 17 33096813 intron variant A/G snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs4794977
rs4794977 		17 33920566 intron variant C/G snv 0.49
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs4795744
rs4795744 		1.000 0.040 17 33098420 intron variant T/C snv 0.82
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs7213721
rs7213721 		17 33292327 5 prime UTR variant G/T snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs72819126
rs72819126 		17 33158862 intron variant G/A snv 1.7E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs72819126
rs72819126 		17 33158862 intron variant G/A snv 1.7E-02
CUI: C0037369
Disease: Smoking
Smoking 		Behavior and Behavior Mechanisms 0.700 1.000 1 2015 2015
dbSNP: rs73982435
rs73982435 		17 33146437 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs870589
rs870589 		17 33287436 intron variant T/A snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs9892479
rs9892479 		1.000 0.040 17 33094883 intron variant G/T snv 4.0E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9903658
rs9903658 		1.000 0.040 17 33729207 intron variant A/G snv 0.11
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs9903658
rs9903658 		1.000 0.040 17 33729207 intron variant A/G snv 0.11
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2019 2019
dbSNP: rs9907580
rs9907580 		1.000 0.080 17 33961449 intron variant T/C snv 0.51
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs9915356
rs9915356 		17 33285476 intron variant A/G;T snv 0.50
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018