Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C/G | Ancestral: C | Ambiguity code: B | MAF: 0.22 (T)

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

Most severe consequence
Missense variant
Evidence status


This variant has 4 synonyms - Show

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3716 sample genotypes and is mentioned in 4 citations.

Variant displays