Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (T)
Location

Chromosome 16:31183958 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 9 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 13 transcripts, has 3981 sample genotypes and is mentioned in 5 citations.

Variant displays