Original source

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

Alleles
AAG/-|MAF: 0.03 (-)
Location

Chromosome 14:103701882-103701884 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 2504 sample genotypes.

Variant displays