Original source

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

Alleles
CTTTC/-|MAF: 0.32 (-)
Location

Chromosome 8:118935562-118935566 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 2596 sample genotypes and is mentioned in 1 citation.

Variant displays