Product Details

SNP ID

rs6786491

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:191202580 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGGCTAGCTTAATGTAATTATGATG[C/T]AAGATTTTGATCAAATATTTTATAT

Phenotype

MIM: 610280

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

OSTN PubMed Links

Gene Details

Gene

OSTN

Gene Name

osteocrin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005247428.4		Intron			XP_005247485.1
XM_017006303.1		Intron			XP_016861792.1

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