Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.30 (T)
Location

Chromosome 5:150848436 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073146

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs58485015

This variant has 2 HGVS names - click the plus to show

5:g.150848436C>T
ENST00000522154.1:c.313C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts, has 2536 sample genotypes, is associated with 2 phenotypes and is mentioned in 32 citations.

Variant displays