Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 308, 2009_August_001_001_AGT_106150_0003

This variation has 3 HGVS names - click the plus to show

About this variant

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

Variation displays