Original source

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

Alleles
G/C/T|Ancestral: G|Ambiguity code: B
Location

Chromosome 4:54101631 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 32 sample genotypes.

Variant displays