Original source

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

Alleles
CAAAA/-
Location

Chromosome 6:161647855-161647859 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 1 sample genotype.

Variant displays