Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.01 (-)
Location

Chromosome 1:186681867 (forward strand) | View in location tab

Co-located

with dbSNP rs181400790 (A/T)

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.186681867delA

Variation displays