This variant maps to 3 locations

Select a location:
Original source

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

Alleles
A/C/T|Ambiguity code: H|MAF: 0.15 (A)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 1 regulatory feature and has 2514 sample genotypes.

Variant displays