Original source

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

Alleles
A/C/G | Ancestral: A | Ambiguity code: V
Location

Chromosome 11:2160829 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM074289, CM830002

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 30 HGVS names - click the plus to show

Variation displays