Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 1:230705933 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 308, 2009_August_001_001_AGT_106150_0003

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and is associated with 2 phenotypes.

Variant displays