Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.29 (A)
Location

Chromosome 20:63718234 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57496318, rs11086125

HGVS names

This variant has 11 HGVS names - Hide

20:g.63718234A>G
ENST00000328969.5:c.584+9070A>G
ENST00000448100.6:c.584+9070A>G
ENST00000357119.8:c.584+9070A>G
ENST00000478385.5:n.167+9070A>G
ENST00000490623.3:c.301+9070A>G
ENST00000355969.10:c.584+9070A>G
ENST00000472711.5:n.284+9070A>G
ENST00000477340.5:n.692+9070A>G
ENST00000369967.7:c.584+9070A>G
ENST00000468235.1:n.76+9070A>G

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3965 sample genotypes, is associated with 2 phenotypes and is mentioned in 19 citations.

Variant displays