Original source

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

C/A/G | Ancestral: C | Ambiguity code: V

Chromosome 1:109548783 (forward strand) | View in location tab

Most severe consequence
Synonymous variant

Archive dbSNP rs45553831

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and 1 regulatory feature.

Variant displays