Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.18 (T)
Location

Chromosome 2:232542288 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 3 HGVS names - click the plus to show

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

About this variant

This variant overlaps 3 transcripts, has 4310 individual genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variation displays