Original source

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

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and 1 regulatory feature.

Variant displays