Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 3:129061951 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM970691

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4761

This variation has 3 HGVS names - click the plus to show

Variation displays