Original source

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

C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (G)

Chromosome 2:219251338 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 52 transcripts and has 2504 sample genotypes.

Variant displays