Original source

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

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 2504 sample genotypes.

Variant displays