Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome 11:2905340 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM994036, CM096711, CD096712

Most severe consequence
Clinical significance

Synonyms

LSDB 33485, 33484

This variation has 24 HGVS names - click the plus to show

Variation displays