Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.16 (T)
Location

Chromosome 2:219251787 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs60515734

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

About this variant

This variant overlaps 25 transcripts and has 2602 sample genotypes.

Variant displays