Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)
Location

Chromosome 5:156486408 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs62381164

HGVS name

5:g.156486408C>T

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays