Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000018.8:g.6940940G>A

This variation has 5 HGVS names - click the plus to show

About this variant

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

Variation displays