This variant maps to 2 locations

Select a location:
Original source

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

Alleles
C/G/T|Ancestral: C|Ambiguity code: B
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

This variant has 5 synonyms - Show

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

Variant displays