Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 11:45802534 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386446178

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

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays