Original source

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

This variant has 3 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2939 sample genotypes and is mentioned in 13 citations.

Variant displays