Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.42 (A)
Location

Chromosome 17:7281743 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs222845, rs59378065

This variant has 4 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2776 sample genotypes and is mentioned in 2 citations.

Variant displays