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 8:132866641 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

8:g.132866641G>A

Variation displays