This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome 11:2159919 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970784, CM920374, CM850007

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 36 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays