Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 22:40344578 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

22:g.40344578delT

Variation displays