Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

This variation has 11 HGVS names - click the plus to show

20:g.63712604T>G
ENST00000448100.5:c.584+3440T>G
ENST00000477340.4:n.692+3440T>G
ENST00000328969.5:c.584+3440T>G
ENST00000357119.7:c.584+3440T>G
ENST00000478385.4:n.167+3440T>G
ENST00000355969.9:c.584+3440T>G
ENST00000490623.2:c.301+3440T>G
ENST00000472711.4:n.284+3440T>G
ENST00000369967.6:c.584+3440T>G
ENST00000468235.1:n.76+3440T>G

This variation has assays on 11 chips - click the plus to show

About this variant

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

Variation displays