Original source

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

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

Chromosome 11:19188245 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030828

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 9566, 2010_April_001_033_CSRP3_600824_0002

This variation has 8 HGVS names - click the plus to show

Variation displays