Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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