Original source

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

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

Chromosome 11:69810559 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM070118

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4467, NM_005247.2:c.466T>C

This variation has 3 HGVS names - click the plus to show

Variation displays