Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status


Archive dbSNP rs3204607

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

About this variant

This variant overlaps 45 transcripts and has 2 individual genotypes.

Variation displays