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
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.48 (C)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 1 regulatory feature and has 2536 sample genotypes.

Variant displays