Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 14:104769372 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs17366125, rs3189474

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 2 sample genotypes.

Variant displays