Original source

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

Alleles
CTGA/-
Location

Chromosome 6:32635412-32635415 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs76136056, rs148144712

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 1 sample genotype.

Variant displays