Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
AAGT/-
Location

Chromosome 9:37426653-37426656 (forward strand) | View in location tab

Most severe consequence
 
Splice donor variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays