Original source

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

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

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

Most severe consequence
 
Synonymous variant
Synonyms

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