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: rs7076156
rs7076156
ZNF365 ; LOC105378327
0.925 0.120 10 62655424 missense variant A/C;G snv 0.80
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2011 2012
dbSNP: rs10995245
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.800 1.000 2 2013 2013
dbSNP: rs10995170
rs10995170
ZNF365
10 62463624 intron variant T/C snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.800 1.000 1 2012 2012
dbSNP: rs10995251
rs10995251
ZNF365 ; LOC105378327
1.000 0.120 10 62638706 intron variant C/T snv 0.29
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.800 1.000 1 2012 2012
dbSNP: rs7089814
rs7089814
ZNF365
10 62427805 intron variant C/G;T snv
CUI: C0425782
Disease: Breast size
Breast size 		0.800 1.000 1 2012 2012
dbSNP: rs10995190
rs10995190
ZNF365
0.882 0.080 10 62518923 intron variant G/A snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.770 1.000 4 2010 2017
dbSNP: rs10822013
rs10822013
ZNF365
0.851 0.080 10 62492218 intron variant C/T snv 0.42
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.720 1.000 1 2011 2016
dbSNP: rs16917546
rs16917546
ZNF365 ; LOC105378327
0.851 0.040 10 62637778 intron variant T/C snv 0.29
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 2 2018 2019
dbSNP: rs7915131
rs7915131
ZNF365
1.000 0.040 10 62658896 non coding transcript exon variant C/T snv 0.53
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 2 2017 2019
dbSNP: rs10761648
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2016 2016
dbSNP: rs10761648
rs10761648
ZNF365
0.827 0.120 10 62594503 intron variant C/T snv 0.20
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2016 2016
dbSNP: rs10822037
rs10822037
ZNF365
1.000 0.040 10 62616798 intron variant T/C snv 0.71
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
dbSNP: rs10995201
rs10995201
ZNF365
1.000 0.080 10 62540131 intron variant A/G snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.700 1.000 1 2017 2017
dbSNP: rs10995240
rs10995240
ZNF365 ; LOC105378327
10 62628871 intron variant G/C snv 0.29
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs10995240
rs10995240
ZNF365 ; LOC105378327
10 62628871 intron variant G/C snv 0.29
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs10995245
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2019 2019
dbSNP: rs10995245
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		0.700 1.000 1 2019 2019
dbSNP: rs10995249
rs10995249
ZNF365 ; LOC105378327
10 62637156 intron variant C/T snv 0.29
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs10995255
rs10995255
ZNF365 ; LOC105378327
0.882 0.040 10 62642673 intron variant G/A snv 0.29
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		0.700 1.000 1 2019 2019
dbSNP: rs10995255
rs10995255
ZNF365 ; LOC105378327
0.882 0.040 10 62642673 intron variant G/A snv 0.29
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		0.700 1.000 1 2019 2019
dbSNP: rs10995255
rs10995255
ZNF365 ; LOC105378327
0.882 0.040 10 62642673 intron variant G/A snv 0.29
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		0.700 1.000 1 2019 2019
dbSNP: rs11598767
rs11598767
ZNF365
1.000 0.040 10 62421587 intron variant T/C snv 3.0E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019