Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 1:16993645 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_058457

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is mentioned in 1 citation.

Variation displays