Original source

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

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

Chromosome 2:27312992 (forward strand) | View in location tab

Most severe consequence
 
Splice donor variant
Evidence status

Clinical significance

Synonyms

LSDB NM_002437.4:c.186+2T>C

This variant has 19 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 23 transcripts and is associated with 1 phenotype.

Variant displays