BCL2L13, BCL2 like 13, 23786

N. diseases: 18; 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: rs13058451
rs13058451 		22 17685093 intron variant T/C;G snv
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs140179402
rs140179402 		1.000 0.080 22 17685512 intron variant C/T snv 1.2E-02
CUI: C0201968
Disease: Cortisol Measurement
Cortisol Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs140179402
rs140179402 		1.000 0.080 22 17685512 intron variant C/T snv 1.2E-02
CUI: C0264408
Disease: Childhood asthma
Childhood asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs34891900
rs34891900 		22 17680392 intron variant C/G;T snv
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs34891900
rs34891900 		22 17680392 intron variant C/G;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs4819618
rs4819618 		22 17651042 intron variant G/A;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs4819618
rs4819618 		22 17651042 intron variant G/A;T snv
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs5013026
rs5013026 		22 17688884 intron variant C/T snv 0.51
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs5747327
rs5747327 		22 17686446 intron variant T/A;C;G snv
CUI: C0857490
Disease: Granulocyte count
Granulocyte count 		0.700 1.000 1 2016 2016