Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 6:129618874 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981162 ; PhenCode LAMA2:c.2901C>A (C/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4041, NM_000426.3:c.2901C>A

This variation has 6 HGVS names - click the plus to show

Variation displays