Original source

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

Alleles
G/A/T | Ambiguity code: D | MAF: 0.47 (G)
Location

Chromosome 2:210294947 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59672906

This variation has 10 HGVS names - click the plus to show

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

About this variant

This variant overlaps 8 transcripts and has 4030 individual genotypes.

Variation displays