Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.04 (G)
Location

Chromosome 16:74713059 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61721968

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3472 sample genotypes.

Variant displays