2[s_discriminator] AND (phs001479.v1.p1[s_ancestor] AND (2[s_discrimin - dbGaP - NCBI

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Clinical Variable	Dataset	Variable Description	Variable ID
AFFECTION_STATUS Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject Subject - Consent Information	Case (Mutation in STAT5B protein) - control status of the subject	phv00386912.v1.p1
MOTHER Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Pedigree Pedigree Information	Mother's Subject ID	phv00386915.v1.p1
ANALYTE_TYPE Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample_Attributes Sample Attribute Information	Analyte Type	phv00386934.v1.p1
Autoimmunity Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Diagnosis criteria - autoimmunity	phv00386931.v1.p1
Leukocytosis Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Diagnosis criteria - leukocytosis	phv00386926.v1.p1
Sex Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Gender of participant	phv00386923.v1.p1
SAMPLE_USE Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample Subject - Sample Mapping - Sample Use information	Sample Use	phv00386920.v1.p1
SEX Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Pedigree Pedigree Information	Sex	phv00386917.v1.p1
SUBJECT_ID Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Pedigree Pedigree Information	Unique Subject ID	phv00386914.v1.p1
CONSENT Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject Subject - Consent Information	Consent group as determined by DAC	phv00386911.v1.p1
SAMPLE_ID Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample_Attributes Sample Attribute Information	De-identified Sample ID	phv00386932.v1.p1
Granulomas Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Diagnosis criteria - granulomas	phv00386929.v1.p1
IS_TUMOR Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample_Attributes Sample Attribute Information	Tumor status	phv00386935.v1.p1
Splenomegaly Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Diagnosis criteria - splenomegaly	phv00386928.v1.p1
STAT5B Q206R Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject_Phenotypes The dataset provides information about study participants' (n=2) diagnosis criteria (yes/no), e.g. leukocytosis, ganulomas, splenomegaly, etc, and basic sociodemographic data.	Diagnosis criteria - deleterious variant	phv00386925.v1.p1
SUBJECT_ID Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample Subject - Sample Mapping - Sample Use information	Subject ID	phv00386918.v1.p1
BODY_SITE Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample_Attributes Sample Attribute Information	Body site where sample was collected	phv00386933.v1.p1
FAMILY_ID Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Pedigree Pedigree Information	Family ID	phv00386913.v1.p1
GENOTYPING_CENTER Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Sample_Attributes Sample Attribute Information	Name of the center which conducted genotyping	phv00386936.v1.p1
SUBJECT_ID Heterozygous Missense Mutation in the Coiled-Coil Domain of STAT5B	STAT5B_Subject Subject - Consent Information	Subject ID	phv00386910.v1.p1

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2[s_discriminator] AND (phs001479.v1.p1[s_ancestor] AND (2[s_disc... (27)
2[s_discriminator] AND (phs001479.v1.p1[s_ancestor] AND (2[s_discriminator] OR (1[s_discriminator] AND 1[s_has_variable])))
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dbGaP
TNFSF10 TNF superfamily member 10 [Homo sapiens]
TNFSF10 TNF superfamily member 10 [Homo sapiens]
Gene ID:8743

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