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 | MAF: 0.01 (T)
Location

Chromosome 11:17509497 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 28936191

This variation has 21 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5, Illumina_Cardio-Metabo_Chip

Variation displays