GPR161, G protein-coupled receptor 161, 23432

N. diseases: 40; N. variants: 9
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: rs10489208
rs10489208 		1 168125471 intron variant C/T snv 0.11
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10918822
rs10918822 		1.000 0.040 1 168079991 3 prime UTR variant T/C snv 6.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs12097632
rs12097632 		1.000 0.040 1 168080802 3 prime UTR variant C/A;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs275137
rs275137 		1.000 0.040 1 168082028 3 prime UTR variant C/A snv 0.47
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs275147
rs275147 		1.000 0.040 1 168089033 non coding transcript exon variant A/G snv 8.3E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs275154
rs275154 		1.000 0.040 1 168092539 intron variant A/G snv 2.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs60504827
rs60504827 		1.000 0.080 1 168127440 intron variant C/T snv 0.16
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2017 2017
dbSNP: rs78320035
rs78320035 		1 168134378 intron variant G/C snv 3.0E-02
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2016 2016
dbSNP: rs78320035
rs78320035 		1 168134378 intron variant G/C snv 3.0E-02
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2016 2016
dbSNP: rs200635937
rs200635937 		0.925 0.040 1 168104855 missense variant A/T snv 2.9E-03 8.0E-04
CUI: C0349588
Disease: Short stature
Short stature 		0.700 0
dbSNP: rs200635937
rs200635937 		0.925 0.040 1 168104855 missense variant A/T snv 2.9E-03 8.0E-04
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		0.700 0
dbSNP: rs200635937
rs200635937 		0.925 0.040 1 168104855 missense variant A/T snv 2.9E-03 8.0E-04
CUI: C4053775
Disease: Pituitary stalk interruption syndrome
Pituitary stalk interruption syndrome 		Pathological Conditions, Signs and Symptoms 0.700 0