Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.37 (A)
Location

Chromosome 5:132660808 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs59327150

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 4122 sample genotypes and is mentioned in 13 citations.

Variant displays