Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.28 (C)
Location

Chromosome 2:55865477 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

2:g.55865477C>T

This variation has assays on 11 chips - click the plus to show

Variation displays