This variation 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

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

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


with HGMD-PUBLIC CM910041, CM910040, CM003587

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

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

About this variant

This variant overlaps 27 transcripts, has 1 individual genotype, is associated with 7 phenotypes and is mentioned in 5 citations.

Variation displays