Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M
Location

Chromosome 2:9548154 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs2949462

This variation has 5 HGVS names - click the plus to show

Variation displays