ZFHX4-AS1, ZFHX4 antisense RNA 1, 100192378

N. diseases: 9; N. variants: 6
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: rs10093547
rs10093547 		0.882 0.040 8 76562310 intron variant T/G snv 0.12
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10093547
rs10093547 		0.882 0.040 8 76562310 intron variant T/G snv 0.12
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10093547
rs10093547 		0.882 0.040 8 76562310 intron variant T/G snv 0.12
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		Neoplasms 0.700 1.000 1 2016 2016
dbSNP: rs10808812
rs10808812 		0.925 0.120 8 76593073 intron variant T/C snv 0.23
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10808812
rs10808812 		0.925 0.120 8 76593073 intron variant T/C snv 0.23
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases 0.700 1.000 1 2017 2017
dbSNP: rs10808813
rs10808813 		1.000 0.080 8 76604707 intron variant C/G;T snv
CUI: C0002170
Disease: Alopecia
Alopecia 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs28727938
rs28727938 		0.882 0.040 8 76566304 intron variant C/G snv 1.0E-01
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs28727938
rs28727938 		0.882 0.040 8 76566304 intron variant C/G snv 1.0E-01
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs28727938
rs28727938 		0.882 0.040 8 76566304 intron variant C/G snv 1.0E-01
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs35251485
rs35251485 		0.882 0.040 8 76571195 intron variant G/A snv 1.0E-01
CUI: C0206710
Disease: Basal Cell Neoplasm
Basal Cell Neoplasm 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs35251485
rs35251485 		0.882 0.040 8 76571195 intron variant G/A snv 1.0E-01
CUI: C0751676
Disease: Basal Cell Cancer
Basal Cell Cancer 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs35251485
rs35251485 		0.882 0.040 8 76571195 intron variant G/A snv 1.0E-01
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		Neoplasms 0.700 1.000 1 2019 2019
dbSNP: rs7838781
rs7838781 		8 76676481 intron variant A/G snv 0.34
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 1 2019 2019