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 19:49061735 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM096280

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4295

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 10 transcripts, has 2530 individual genotypes and is associated with 2 phenotypes.

Variation displays