Original source

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

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

Chromosome 1:186671690 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.186671690delT

Variation displays