Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/T | Ancestral: G | Ambiguity code: K

Chromosome 1:161231120 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Archive dbSNP rs3204607

This variant has 47 HGVS names - click the plus to show

About this variant

This variant overlaps 45 transcripts and has 2 sample genotypes.

Variant displays