Original source

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

C/A/G | Ancestral: C | Ambiguity code: V

Chromosome 4:73413602 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB OrebroSW, 187

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 36 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays