Original source

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

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

Chromosome 11:47337729 (forward strand) | View in location tab


with HGMD-PUBLIC CM043543

Most severe consequence
Evidence status

Clinical significance


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

About this variant

This variant overlaps 10 transcripts, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays