Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)
Location

Chromosome 1:43338634 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM002058

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4169, 2009_August_001_173_MPL_159530_0005

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts, has 2504 individual genotypes and is associated with 3 phenotypes.

Variation displays