This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 21:25891784 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM910041, CM910040, CM003587

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 9 synonyms - click the plus to show

This variant has 54 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 1 sample genotype, is associated with 8 phenotypes and is mentioned in 5 citations.

Variant displays