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: rs11001819
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.800 1.000 3 2011 2015
dbSNP: rs2637254
rs2637254
LRMDA
10 76552244 intron variant G/A snv 0.44
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 3 2017 2019
dbSNP: rs11001819
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		0.700 1.000 2 2011 2012
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C0162311
Disease: Androgenetic Alopecia
Androgenetic Alopecia 		0.700 1.000 2 2016 2017
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 2 2016 2017
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C2676272
Disease: Alopecia, Androgenetic, 3
Alopecia, Androgenetic, 3 		0.700 1.000 2 2016 2017
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C4049090
Disease: Alopecia, Androgenetic, 1
Alopecia, Androgenetic, 1 		0.700 1.000 2 2016 2017
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C2678038
Disease: Alopecia, Androgenetic, 2
Alopecia, Androgenetic, 2 		0.700 1.000 2 2016 2017
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C0029489
Disease: Other alopecia
Other alopecia 		0.700 1.000 2 2016 2017
dbSNP: rs2637254
rs2637254
LRMDA
10 76552244 intron variant G/A snv 0.44
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		0.700 1.000 2 2017 2019
dbSNP: rs10458660
rs10458660
LRMDA
1.000 0.080 10 76176818 intron variant A/G snv 0.19
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs10824347
rs10824347
LRMDA
10 75885471 intron variant A/T snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs10824380
rs10824380
LRMDA
10 76178160 intron variant A/G snv 0.37
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs11001398
rs11001398
LRMDA
10 75461756 intron variant G/A;C snv
CUI: C0424678
Disease: Lean body mass
Lean body mass 		0.700 1.000 1 2019 2019
dbSNP: rs11001667
rs11001667
LRMDA
1.000 0.080 10 76175587 intron variant A/G snv 0.18
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs11593840
rs11593840
LRMDA
0.807 0.080 10 76436854 intron variant A/G snv 0.40
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs12764182
rs12764182
LRMDA
10 76131488 intron variant T/G snv 0.16
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs1873465
rs1873465
LRMDA
1.000 0.080 10 76430201 intron variant C/T snv 0.84
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs1875163
rs1875163
LRMDA ; LOC105378367
0.925 0.040 10 75716885 intron variant A/G snv 4.0E-02
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
dbSNP: rs1875163
rs1875163
LRMDA ; LOC105378367
0.925 0.040 10 75716885 intron variant A/G snv 4.0E-02
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs1907350
rs1907350
LRMDA
1.000 0.080 10 76435054 intron variant A/G snv 0.41
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs1992011
rs1992011
LRMDA
10 75986895 intron variant T/C snv 0.42
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2019 2019
dbSNP: rs2146595
rs2146595
LRMDA
10 75874476 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2579762
rs2579762
LRMDA
1.000 0.040 10 76559121 3 prime UTR variant A/C snv 0.39
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2019 2019
dbSNP: rs2637254
rs2637254
LRMDA
10 76552244 intron variant G/A snv 0.44
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		0.700 1.000 1 2019 2019