Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.13 (A)

Chromosome 1:231407996 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs849808

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 4756 individual genotypes.

Variation displays