Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 12:52952785 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NC_000012.10:g.51632836G>T

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 32 transcripts and is associated with 1 phenotype.

Variant displays