This variant maps to 2 locations

Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

Synonyms

LSDB NM_000157.2:c.1504C>T, 13821

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant is associated with 14 phenotypes and is mentioned in 2 citations.

Variant displays