Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.28 (T)
Location

Chromosome 5:150227998 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073146

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58485015

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

5:g.150227998C>T
ENST00000522154.1:c.313C>T

Genotyping chips

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

Variation displays