Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 19:33301702 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NM_004364.3:c.713C>A

HGVS names

This variant has 7 HGVS names - Show

About this variant

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

Variant displays