Original source

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

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

Chromosome 11:44267585 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002931

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 13163, 2010_April_001_008_ALX4_605420_0005

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

Variation displays