Original source

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

Alleles
TCTG/-
Location

Chromosome 3:8745701-8745704 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays