Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.31 (G)

Chromosome 1:231408034 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs849809

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

About this variant

This variant overlaps 3 transcripts, has 3624 individual genotypes and is mentioned in 3 citations.

Variation displays