Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)
Location

Chromosome 2:208121913 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 2 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3716 sample genotypes and is mentioned in 4 citations.

Variant displays