Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 11:47356628 (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: Illumina_ExomeChip

Variation displays