Original source

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

Alleles
A/-/AA | Ancestral: A
Location

Chromosome 4:56393335 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs79100315

This variation has 2 HGVS names - click the plus to show

Variation displays