Original source

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

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 25 transcripts and has 2602 sample genotypes.

Variant displays