Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 5:151851470 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM992336

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2270, NM_000171.3:c.832C>A

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

Variation displays