Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.14 (T)
Location

Chromosome 21:36461009 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 8 HGVS names - click the plus to show

21:g.36461009C>T
ENST00000342108.2:c.687G>A
ENST00000399136.5:c.687G>A
ENST00000428667.1:n.277+15002C>T
ENST00000399135.5:c.687G>A
ENST00000399139.5:c.687G>A
ENST00000429588.1:n.54-19222C>T
ENST00000399137.5:c.687G>A

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2857 sample genotypes, is associated with 2 phenotypes and is mentioned in 6 citations.

Variant displays