Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)

Chromosome 15:71811591 (forward strand) | View in location tab


with dbSNP rs772903026 (G/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2010_April_001_034_NR2E3_604485_0003, 12682

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays