Original source

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

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

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

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


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