Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.32 (A)
Location

Chromosome 3:36993455 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR045225

Most severe consequence
 
5 prime UTR variant
Evidence status

Clinical significance

Synonyms

This variant has 5 HGVS names - click the plus to show

3:g.36993455G>A
ENST00000231790.6:c.-93G>A
ENST00000536378.5:c.-725G>A
LRG_216:g.5106G>A
LRG_216t1:c.-93G>A

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, 1 regulatory feature, has 2684 sample genotypes, is associated with 2 phenotypes and is mentioned in 41 citations.

Variant displays