Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.16 (-)
Location

Chromosome 5:135027464 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

5:g.135027464delG

Variation displays