Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.12 (G)
Location

Chromosome 14:90713721 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386481205

HGVS names

This variant has 3 HGVS names - Hide

14:g.90713721A>G
ENST00000557766.1:c.393-14498T>C
ENST00000328459.10:c.698+16354T>C

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3687 sample genotypes.

Variant displays