Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:67490910 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061635

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_003977.2:c.910C>T, 2010_April_001_003_AIP_605555_0003, 13279

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

Variation displays