Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 11:67487155 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS104882

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.249G>T

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

Variation displays