Explore this variant
Genomic context
- Genes and regulation
- Flanking sequence
Population genetics
Phenotype data
Sample genotypes
Linkage disequilibrium
Phylogenetic context
Citations
3D Protein model

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rs3510773852 SNP

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Most severe consequence

intergenic variant

Alleles

C/A

Location

Primary_assembly LG1:36795 (forward strand)|VCF:LG1 36795 rs3510773852 C A

HGVS name

NC_031965.2:g.36795C>A

Original source

Variants from EVA (release 5)|View in EVA

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Explore this variant

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Graphical neighbourhood region

Consequences (e.g. missense) (Not available)

Upstream and downstream sequence

Allele and genotype frequencies by population (Not available)

Diseases and traits (Not available)

Sample genotypes (Not available)

LD plots and tables (Not available)

Sequence conservation via cross-species alignments (Not available)

Citations (Not available)

3D Protein model (Not available)

Using the website

Video: Browsing SNPs and CNVs in Ensembl
Video: Clip: Genome Variation
Video: BioMart: Variation IDs to HGNC Symbols
Exercise: Genomes and SNPs in Malaria

Analysing your data

Test your own variants with the Variant Effect Predictor

Programmatic access

Tutorial: Accessing variation data with the Variation API

Reference materials

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Personal Data