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SNP ID:
rs855768
Gene
EMX2 EMX2OS
Gene Name
Set Membership:
> Validated
Chromosome Location:
Chr.10: 117547956 - 117547956 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CTTAGGACTTGCATCTCGGGGGCTG[A/G]GTCTTTGCTGAGTCTGGAACTGGAG

Assay ID C____856249_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 600035 MIM: 607637

Literature Links:

 EMX2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
T (0.15)
(0.85)
Caucasian
A (0.08)
(0.92)
CEPH (CEU) - Not Available
EAS
T (0.23)
(0.77)
African American
A (0.27)
(0.73)
YRI (Yoruba) - Not Available
SAS
T (0.06)
(0.94)
Japanese
A (0.27)
(0.73)
CHB (Han Chinese) - Not Available
AFR
T (0.22)
(0.78)
Chinese
A (0.14)
(0.86)
JPT (Japanese) - Not Available
EUR
T (0.09)
(0.91)
AMR
T (0.12)
(0.88)
EMX2 - empty spiracles homeobox 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001165924.1 Intron NP_001159396.1
NM_004098.3 Intron NP_004089.1
EMX2OS - EMX2 opposite strand/antisense RNA
There are no transcripts associated with this gene.

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