Original source

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

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

Chromosome 16:50699751 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance


Infevers 330

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

About this variant

This variant overlaps 7 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays