Original source

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

This variant has 3 HGVS names - click the plus to show

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

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 3687 sample genotypes.

Variant displays