Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D
Location

Chromosome 15:91346951 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS073439 ; PhenCode BLMbase_D0004:g.87317G>A (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_000057.2:c.3558+1G>A

This variation has 16 HGVS names - click the plus to show

Variation displays