Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 4:154563022 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_014169

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts and has 263 individual genotypes.

Variation displays