Original source

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

This variant has 3 HGVS names - click the plus to show

About this variant

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

Variant displays