Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 5:151851406 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086829, CM940872, CM940871

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2264, NM_000171.3:c.896G>A, 2265, NM_000171.3:c.896G>T

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

Variation displays