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

This variation maps to 3 genomic locations; None selected

Evidence status

This variation has 2 synonyms - click the plus to show

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays