Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 1:16997049 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_058454

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and is mentioned in 1 citation.

Variation displays