Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 16:50699481 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS061257

Most severe consequence
Evidence status

Clinical significance

Synonyms

Infevers 194

This variation has 8 HGVS names - click the plus to show

Variation displays