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
Location

Chromosome 5:151851440 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM013549

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000171.3:c.862G>A, 2274

This variation has 7 HGVS names - click the plus to show

Variation displays