Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 12:13562998 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.11:g.13715932C>A

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 2 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays