Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.12 (C)
Location

Chromosome 2:207552876 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61490155

This variation has 9 HGVS names - click the plus to show

Variation displays