Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 2:27309707 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3189966

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

About this variant

This variant overlaps 25 transcripts and has 1 individual genotype.

Variation displays