This variation has been flagged

Variation has more than 3 different alleles

Select a location:
Original source

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

Alleles
C/A/G/T | Ambiguity code: N | MAF: 0.22 (T)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

This variation has 8 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni1-Quad

Variation displays