This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

A/C/G/T | Ancestral: A | Ambiguity code: N

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


with HGMD-PUBLIC CM043543

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB MYBPC3_2374T_C_121010

This variant has 36 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 15 transcripts, is associated with 3 phenotypes and is mentioned in 2 citations.

Variant displays