Original source

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

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

Chromosome 12:110913316 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961006 ; PhenCode MYL2:c.283C>G (G/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

Variation displays