Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 16:88810494 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM044206

Most severe consequence
Synonyms

Uniprot VAR_069050

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

Variation displays