Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 7:55201204 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

Uniprot VAR_019300

This variant has 11 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 3098 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays