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
Location

Chromosome 14:30877806 (forward strand) | View in location tab

Co-located

with dbSNP rs369313054 (T/-)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays