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: 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: 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: 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: 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: 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: 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: rs72642263
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2019 2019
dbSNP: rs72642263
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2019 2019
dbSNP: rs72642263
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs72642263
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02
CUI: C0376705
Disease: Viral Load result
Viral Load result 		0.700 1.000 1 2019 2019
dbSNP: rs72642263
rs72642263
LRMDA
1.000 10 76449748 intron variant A/G snv 9.2E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2019 2019
dbSNP: rs9416087
rs9416087
LRMDA
0.925 0.040 10 75596836 intron variant A/G snv 0.58
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs9416087
rs9416087
LRMDA
0.925 0.040 10 75596836 intron variant A/G snv 0.58
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.700 1.000 1 2018 2018
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: rs3012053
rs3012053
LRMDA
10 75533351 intron variant A/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
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: rs4746339
rs4746339
LRMDA
10 75896751 intron variant A/T snv 0.76
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019