Original source

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

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

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

Most severe consequence
Non coding transcript exon variant
Evidence status


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