Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 21:37833307 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

21:g.37833307C>T
ENST00000399136.1:c.687G>A
ENST00000342108.2:c.687G>A
ENST00000428667.1:n.277+15002C>T
ENST00000399135.1:c.687G>A
ENST00000399139.1:c.687G>A
ENST00000429588.1:n.54-19222C>T
ENST00000399137.1:c.687G>A

This variation has assays on 5 chips - click the plus to show

Variation displays