Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.01 (T)
Location

Chromosome 5:132867052 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

Synonyms

ClinVar SCV000169721

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays