Human (GRCh37.p13)
Most severe consequence
 
frameshift variant
Alleles
GCGGA/-|Ancestral: GCGGA
Location

Chromosome 5:139493770-139493774 (forward strand)|VCF:5  139493769  rs793888537  GGCGGA  G

Evidence status

Clinical significance

HGVS names

This variant has 5 HGVS names - Show

Synonyms

This variant has 2 synonyms - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, is associated with 1 phenotype and is mentioned in 1 citation.

Description from SNPedia

Description not available [More information from SNPedia]