Original source

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

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

Chromosome 16:23637756 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

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

Variation displays