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: 0.40 (A)
Location

Chromosome 15:24990569 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56619905, rs12913018

This variation has 5 HGVS names - click the plus to show

15:g.24990569G>A
ENST00000557230.1:c.*400-8401G>A
ENST00000551631.4:n.888-7797G>A
ENST00000551312.4:c.*953+8132G>A
ENST00000551361.1:n.444+8132G>A

This variation has assays on 7 chips - click the plus to show

Variation displays