Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.15 (T)
Location

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

21:g.36461009C>T
ENST00000399136.3:c.687G>A
ENST00000342108.2:c.687G>A
ENST00000428667.1:n.277+15002C>T
ENST00000399135.3:c.687G>A
ENST00000399139.3:c.687G>A
ENST00000429588.1:n.54-19222C>T
ENST00000399137.3:c.687G>A

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

Variation displays