Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.14 (T)
Location

Chromosome 5:157059397 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs62381164

HGVS name

5:g.157059397C>T

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts, has 2506 sample genotypes and is mentioned in 3 citations.

Variant displays