Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.16 (A)
Location

Chromosome 14:97636721 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59239619, rs56505088

HGVS names

This variant has 3 HGVS names - Hide

14:g.97636721G>A
ENST00000355909.7:n.626-3030C>T
ENST00000556163.1:n.473+762C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3864 sample genotypes.

Variant displays