Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | View in dbSNP

Alleles
G/A | Ambiguity code: R
Location

Supercontig Contig5384:16749 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Ensembl ENSOANSNP1

HGVS name

Contig5384:g.16749G>A

Variation displays