Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: < 0.01 (A)
Location

Chromosome 16:50733392 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS061257

Most severe consequence
Evidence status

Synonyms

Infevers 194

This variation has 13 HGVS names - click the plus to show

Variation displays