Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 8 HGVS names - Hide

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 3042 sample genotypes and is mentioned in 1 citation.

Variant displays