Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 11:47359280 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043543

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYBPC3_2374T_C_121010

This variation has 24 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays