Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 1:16986179 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status


Archive dbSNP rs3205048

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2 sample genotypes.

Variant displays