Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 21:42388983 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM054156

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 11613314

This variant has 11 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2505 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays