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|MAF: < 0.01 (T)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NP_000286.3:p.ASP341ASN

HGVS name

None

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant has 2504 sample genotypes, is associated with 8 phenotypes and is mentioned in 1 citation.

Variant displays