Original source

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

Alleles
-/A | MAF: 0.09 (A)
Location

Chromosome 2: between 219252541 and 219252542 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56732349, rs138627203

This variation has 11 HGVS names - click the plus to show

Variation displays