Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 16:23626435 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_024675.3:c.2587-38C>G

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Variation displays