Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.48 (G)
Location

Chromosome 3:115639308 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59103249

This variation has 3 HGVS names - click the plus to show

3:g.115639308G>A
ENST00000393780.3:c.-259+15589G>A
ENST00000305124.7:c.30+15589G>A

This variation has assays on 9 chips - click the plus to show

Variation displays