Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 14:22860237 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

14:g.22860237T>C

This variation has assays on 9 chips - click the plus to show

Variation displays