Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.28 (T)
Location

Chromosome 6:166157676 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3816306, rs60732233

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, has 2774 sample genotypes and is mentioned in 1 citation.

Variant displays