Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.36 (A)
Location

Chromosome 20:3670518 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs17513867, rs1000181

HGVS names

This variant has 8 HGVS names - Hide

20:g.3670518G>A
ENST00000483362.1:n.108C>T
ENST00000356518.6:c.2240+488C>T
ENST00000379861.8:c.2240+488C>T
ENST00000619289.4:c.1880+488C>T
ENST00000466620.5:n.1801+488C>T
ENST00000350009.6:c.2162+488C>T
ENST00000617732.1:c.*927+488C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2599 sample genotypes and is mentioned in 10 citations.

Variant displays