Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.49 (G)
Location

Chromosome 14:104771343 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs59634299

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 20 transcripts, has 4326 sample genotypes and is mentioned in 4 citations.

Variant displays