Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.34 (C)
Location

Chromosome 14:27039812 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17212295, rs60892220

HGVS names

This variant has 2 HGVS names - Hide

14:g.27039812C>G
ENST00000552303.1:n.206-37426C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 transcript and has 6062 sample genotypes.

Variant displays