Original source

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

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

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

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

LSDB NC_000018.8:g.6940940G>A

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays