Original source

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

Alleles
TCAA/-|MAF: 0.01 (-)
Location

Chromosome 4:174491347-174491350 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs140833916

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 2550 sample genotypes.

Variant displays