Original source

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

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

Chromosome 2:165770217 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041346

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 10517

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

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays