Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.38 (C)
Location

Chromosome 3:171027026 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR025511

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386598555

HGVS name

3:g.171027026T>C

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo

About this variant

This variant overlaps 3 transcripts and has 2630 sample genotypes.

Variant displays