Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 15:38322324 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_152594.2:c.291G>A

This variation has 4 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays