This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A/C/T|Ancestral: G|Ambiguity code: N|MAF: 0.41 (G)
Location

Chromosome 21:25917090 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58596776, rs1620916

HGVS names

This variant has 27 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2508 sample genotypes.

Variant displays