Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.16 (G)
Location

Chromosome 3:7796555 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs329055, rs59505890, rs332334

HGVS name

3:g.7796555G>A

This variation has assays on 9 chips - click the plus to show

Variation displays