Source: ALL
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: rs10519227
rs10519227 		15 49454167 intron variant T/A snv 0.20
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		0.800 1.000 1 2013 2013
dbSNP: rs12591300
rs12591300 		1.000 0.040 15 49412544 intron variant G/A snv 0.26
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.710 1.000 1 2011 2011
dbSNP: rs10519227
rs10519227 		15 49454167 intron variant T/A snv 0.20
CUI: C0441683
Disease: Hormone measurement
Hormone measurement 		0.700 1.000 1 2013 2013
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0153368
Disease: Malignant neoplasm of floor of mouth
Malignant neoplasm of floor of mouth 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0153380
Disease: Malignant neoplasm of other specified parts of mouth
Malignant neoplasm of other specified parts of mouth 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0153369
Disease: Malignant neoplasm of anterior portion of floor of mouth
Malignant neoplasm of anterior portion of floor of mouth 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0153407
Disease: Malignant neoplasm of other sites within the lip and oral cavity
Malignant neoplasm of other sites within the lip and oral cavity 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0153381
Disease: Malignant neoplasm of mouth
Malignant neoplasm of mouth 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478 		0.827 0.080 15 49536822 intron variant T/C snv 0.30
CUI: C0496758
Disease: Malignant neoplasm of lateral floor of mouth
Malignant neoplasm of lateral floor of mouth 		Neoplasms; Stomatognathic Diseases 0.700 1.000 1 2016 2016
dbSNP: rs12899680
rs12899680 		15 49579681 intron variant C/G snv 0.44
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs17400427
rs17400427 		1.000 0.040 15 49448874 intron variant T/C snv 0.20
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs17477923
rs17477923 		1.000 0.040 15 49418988 intron variant T/C snv 0.22
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism 		Endocrine System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs35251997
rs35251997 		15 49413948 intron variant A/T snv 6.6E-02
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 1 2019 2019
dbSNP: rs35251997
rs35251997 		15 49413948 intron variant A/T snv 6.6E-02
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs36023246
rs36023246 		15 49407114 intron variant A/G snv 0.28
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs4267253
rs4267253 		15 49547350 intron variant G/A snv 0.31
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs7182948
rs7182948 		1.000 0.040 15 49549483 intron variant A/C;G;T snv
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs10519225
rs10519225 		1.000 0.040 15 49428581 intron variant G/A snv 0.28
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 1.000 1 2012 2012
dbSNP: rs372127537
rs372127537 		0.925 0.040 15 49485006 3 prime UTR variant T/- del 8.4E-05
CUI: C0024636
Disease: Malocclusion
Malocclusion 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs372127537
rs372127537 		0.925 0.040 15 49485006 3 prime UTR variant T/- del 8.4E-05
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		Stomatognathic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs4480740
rs4480740 		1.000 0.040 15 49463645 intron variant G/A snv 0.25
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 1.000 1 2011 2011
dbSNP: rs7170426
rs7170426 		1.000 0.040 15 49459656 intron variant A/G snv 0.32
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		Respiratory Tract Diseases 0.010 1.000 1 2012 2012