Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.26 (T)
Location

Chromosome 2:219252611 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57293506

This variant has 11 HGVS names - click the plus to show

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

About this variant

Variant displays