Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
HGVS names

This variant has 13 HGVS names - Hide

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

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts, has 2857 sample genotypes, is associated with 2 phenotypes and is mentioned in 7 citations.

Variant displays