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: 0.24 (A)
Location

Chromosome 14:104793397 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR108282

Most severe consequence
Evidence status

Synonyms

This variation has 9 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays