SHISA6, shisa family member 6, 388336

N. diseases: 6; N. variants: 12
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: rs2969180
rs2969180 		1.000 17 11504584 intron variant G/A snv 0.34
CUI: C0034951
Disease: Refractive Errors
Refractive Errors 		Eye Diseases 0.710 1.000 2 2013 2014
dbSNP: rs11078889
rs11078889 		1.000 0.040 17 11244223 intron variant A/T snv 0.88
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11078890
rs11078890 		1.000 0.040 17 11251291 intron variant A/G snv 0.83
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs11650677
rs11650677 		17 11328196 intron variant G/A snv 0.26
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs11653055
rs11653055 		1.000 0.040 17 11239318 intron variant T/C snv 0.64
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs205024
rs205024 		17 11324035 intron variant C/T snv 0.35
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs2908972
rs2908972 		1.000 0.040 17 11503942 intron variant T/A snv 0.39
CUI: C0027092
Disease: Myopia
Myopia 		Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2969180
rs2969180 		1.000 17 11504584 intron variant G/A snv 0.34
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction 		0.700 1.000 1 2013 2013
dbSNP: rs4792113
rs4792113 		1.000 0.040 17 11251122 intron variant T/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs6503364
rs6503364 		1.000 0.040 17 11249553 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs8072737
rs8072737 		1.000 0.040 17 11252879 intron variant T/C snv 7.9E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9303273
rs9303273 		1.000 0.040 17 11250522 intron variant A/C;G snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs9916424
rs9916424 		1.000 0.040 17 11250025 intron variant G/A snv 8.4E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017