Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 11:47335077 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086392

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYBPC3_2870C_G_082810

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, has 2504 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays