Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.35 (T)
Location

Chromosome 20:63712604 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Hide

20:g.63712604T>G
ENST00000448100.6:c.584+3440T>G
ENST00000477340.5:n.692+3440T>G
ENST00000328969.5:c.584+3440T>G
ENST00000357119.8:c.584+3440T>G
ENST00000478385.5:n.167+3440T>G
ENST00000490623.3:c.301+3440T>G
ENST00000355969.10:c.584+3440T>G
ENST00000472711.5:n.284+3440T>G
ENST00000369967.7:c.584+3440T>G
ENST00000468235.1:n.76+3440T>G

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 19 transcripts, has 3692 sample genotypes, is associated with 2 phenotypes and is mentioned in 6 citations.

Variant displays