Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.13 (T)
Location

Chromosome 17:17213230 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60776136

This variant has 6 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 3435 sample genotypes.

Variant displays