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rs3363710310 SNP

Most severe consequence
 
intergenic variant
Alleles
T/C
Location

Chromosome 7:1338 (forward strand)|VCF:7  1338  rs3363710310  T  C

HGVS name

NC_006474.4:g.1338T>C

Original source

Variants from EVA (release 6)|View in EVA

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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)

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