Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.05 (G)
Location

Chromosome 10:82273509 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

10:g.82273509A>G
ENST00000602794.5:c.*372-85230A>G
ENST00000555784.5:c.136-85230A>G
ENST00000404576.6:c.236-85230A>G
ENST00000404547.5:c.824-85230A>G
ENST00000556918.5:c.313+40690A>G
ENST00000372142.6:c.161-85230A>G
ENST00000372141.6:c.824-85230A>G

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2635 sample genotypes and is mentioned in 1 citation.

Variant displays