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SNP ID:
rs3367
Gene
-
Gene Name
-
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.21: 45763982 - 45763982 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

AATAATACGGTGTTTTGAATGTCAT[A/G]CATGGCTTTTCCTGTTGAAACATCT

Assay ID C___9481649_1_
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.19)
(0.81)
Caucasian
G (0.26)
(0.74)
CEPH (CEU)
G (0.16)
(0.84)
EAS
G (0.17)
(0.83)
African American
G (0.10)
(0.90)
YRI (Yoruba)
G (0.14)
(0.86)
SAS
G (0.31)
(0.69)
Chinese - Not Available JPT (Japanese)
G (0.14)
(0.86)
AFR
G (0.15)
(0.85)
Japanese - Not Available CHB (Han Chinese)
G (0.20)
(0.80)
EUR
G (0.19)
(0.81)
AMR
G (0.13)
(0.87)

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More Information


Set Membership:

 HapMap Validated

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