Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 2:219250370 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs3204448

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 31 transcripts and has 1 sample genotype.

Variant displays