Product Details

SNP ID

rs9646990

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:70778819 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AATAGAAACCCAGTTTGCTGCTTAA[C/T]ATCTTTAAGAAGGCAGGCACACTCC

Phenotype

MIM: 608697

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FIGLA PubMed Links

Gene Details

Gene

FIGLA

Gene Name

folliculogenesis specific bHLH transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004311.3		Intron			NP_001004311.2

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