Original source

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

Alleles
A/C | Ancestral: T | Ambiguity code: M | MAF: 0.19 (A)
Location

Chromosome 3:55279372 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

3:g.55279372A>C

This variation has assays on 12 chips - click the plus to show

Variation displays