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 13:51946337 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980180

Most severe consequence
Synonyms

Uniprot VAR_000751

This variation has 14 HGVS names - click the plus to show

Variation displays