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: 0.08 (A)
Location

Chromosome 1:12204814 (forward strand) | View in location tab

Co-located

with dbSNP rs375304935 (C/ACAA)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58707651, rs9430687

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

Variation displays