Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 20:50400278 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs74175587

HGVS name

20:g.50400278delA

Variation displays