Assay Details

Species:	Human
dbSNP Submissions:	42 submissions
Phenotype:	MIM: 601769
Literature Links:	VDR PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome

Applied Biosystems^®

HapMap

Global - Not Available

Caucasian - Not Available

CEPH (CEU)

A (0.44)

(0.56)

EAS - Not Available

African American - Not Available

YRI (Yoruba)

A (0.28)

(0.72)

SAS - Not Available

Japanese

T (0.06)

(0.94)

JPT (Japanese)

A (0.12)

(0.88)

AFR - Not Available

Chinese

T (0.03)

(0.97)

CHB (Han Chinese)

A (0.02)

(0.98)

EUR - Not Available

AMR - Not Available

VDR - vitamin D (1,25- dihydroxyvitamin D3) receptor
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_000376.2		Intron			NP_000367.1
NM_001017535.1		Intron			NP_001017535.1
NM_001017536.1		Intron			NP_001017536.1

More Information

Additional Information:

For this assay, SNP rs11574109 is located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the NCBI SNP database (dbSNP). A higher minor allele frequency in your study population represents a higher risk to assay performance.