Original source

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

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

Chromosome 11:111908934 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980447

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 27 HGVS names - click the plus to show

Variation displays