Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.31 (C)
Location

Chromosome 7:2374952 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 7 transcripts and has 3514 sample genotypes.

Variant displays