Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.37 (A)
Location

Chromosome 5:126543216 (forward strand) | View in location tab

Co-located

with dbSNP rs199550747 (C/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58192485

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

Variation displays