This variant has been flagged

Variation has more than 3 different alleles

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C/G/T|Ambiguity code: N|MAF: 0.37 (A)
Location

This variant maps to 5 genomic locations; None selected

Evidence status

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 1 regulatory feature and has 2504 sample genotypes.

Variant displays