Original source

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

Alleles
C/- | MAF: 0.40 (-)
Location

Chromosome 2:232539050 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139006344, rs367681527

HGVS name

2:g.232539050delC

Variation displays