Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 11:47341172 (forward strand) | View in location tab

Co-located

with ClinVar rs397515931 (G/-)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB MYBPC3_1863C_T_121410

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays