Original source

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

Alleles
C/- | Ancestral: C
Location

Chromosome 2:232543488 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377643922

This variation has 3 HGVS names - click the plus to show

Variation displays