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 16:47696408 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CP973613

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 28660_1, NM_000293.2:c.2923T>C

This variation has 8 HGVS names - click the plus to show

Variation displays