Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.29 (C)
Location

Chromosome 15:63059641 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

Synonyms

This variant has 9 synonyms - Show

HGVS names

This variant has 43 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 32 transcripts, has 3810 sample genotypes, is associated with 3 phenotypes and is mentioned in 4 citations.

Variant displays