Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.16 (T)
Location

Chromosome 17:47300211 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57072022

HGVS names

This variant has 5 HGVS names - Hide

17:g.47300211G>T
ENST00000559488.5:c.1914-267G>T
ENST00000560629.1:c.1879-267G>T
LRG_481:g.51370G>T
LRG_481t1:c.1914-267G>T

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 5 transcripts, has 3759 sample genotypes and is mentioned in 2 citations.

Variant displays