Original source

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

Alleles
CCT/-|MAF: 0.26 (-)
Location

Chromosome 14:100845395-100845397 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 2504 sample genotypes.

Variant displays