Original source

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

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

Chromosome 18:6950941 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NC_000018.8:g.6940940G>A

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and is associated with 1 phenotype.

Variant displays