Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs60995570

This variation has 6 HGVS names - click the plus to show

About this variant

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

Variation displays