Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 5:135027988 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs3191669

This variation has 2 HGVS names - click the plus to show

Variation displays