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: rs112912841
rs112912841
LPP
3 188269895 intron variant A/G snv 0.12
CUI: C0015944
Disease: Fetal Membranes, Premature Rupture
Fetal Membranes, Premature Rupture 		0.700 1.000 1 2019 2019
dbSNP: rs11707807
rs11707807
LPP
1.000 0.040 3 188370473 intron variant A/G snv 0.36
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs11719821
rs11719821
LPP
0.882 0.040 3 188370530 intron variant T/C snv 0.36
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs11719821
rs11719821
LPP
0.882 0.040 3 188370530 intron variant T/C snv 0.36
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2019 2019
dbSNP: rs11719821
rs11719821
LPP
0.882 0.040 3 188370530 intron variant T/C snv 0.36
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs12634152
rs12634152
LPP
0.925 0.120 3 188403231 intron variant C/T snv 0.43
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs12634152
rs12634152
LPP
0.925 0.120 3 188403231 intron variant C/T snv 0.43
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		0.700 1.000 1 2019 2019
dbSNP: rs13099273
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs13099273
rs13099273
LPP
1.000 0.080 3 188415730 intron variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs17670280
rs17670280
LPP
1.000 0.080 3 188682451 intron variant G/A;C snv
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs17670280
rs17670280
LPP
1.000 0.080 3 188682451 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs2030519
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs2030520
rs2030520
LPP
3 188401794 intron variant C/G;T snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2889896
rs2889896
LPP
1.000 0.080 3 188384928 intron variant C/T snv 0.43
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs3856920
rs3856920
LPP
3 188823038 intron variant A/G snv 0.25
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4686952
rs4686952
LPP
3 188331054 intron variant G/A snv 0.43
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs4686991
rs4686991
LPP
3 188647490 intron variant A/G;T snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs55661102
rs55661102
LPP
0.925 0.080 3 188683350 intron variant A/G snv 0.13
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs55661102
rs55661102
LPP
0.925 0.080 3 188683350 intron variant A/G snv 0.13
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs60946162
rs60946162
LPP
1.000 0.040 3 188415548 intron variant C/T snv 0.35
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs62289742
rs62289742
LPP ; LPP-AS2
3 188152990 non coding transcript exon variant C/T snv 0.26
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs6444307
rs6444307
LPP
3 188589730 intron variant A/G snv 0.33
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019