Original source

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

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

Chromosome 12:52472119 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 34 sample genotypes.

Variant displays