Original source

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

Alleles
A/C|Ancestral: C|Ambiguity code: M|MAF: < 0.01 (A)
Location

Chromosome 21:34094556 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60995570

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays