Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs62381164

HGVS name

5:g.157059397C>T

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays