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
Evidence status

Clinical significance

Synonyms

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

3:g.36993455G>A
ENST00000231790.5:c.-93G>A
ENST00000536378.4:c.-725G>A
LRG_216:g.5106G>A
LRG_216t1:c.-93G>A

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

About this variant

This variant overlaps 22 transcripts, has 2684 individual genotypes, is associated with 2 phenotypes and is mentioned in 40 citations.

Variation displays