Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 12:13564526 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.11:g.13717460C>T

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and is associated with 1 phenotype.

Variant displays