Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (T)
Location

Chromosome 2:27321418 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 18 HGVS names - click the plus to show

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

About this variant

This variant overlaps 23 transcripts, has 3764 individual genotypes and is mentioned in 1 citation.

Variation displays