Original source

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

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

Chromosome 2:233403760 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs139006344, rs367681527

HGVS name

2:g.233403760delC

Variation displays