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
Location

Chromosome 14:28765973 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

14:g.28765973C>A

Variation displays