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: 0.35 (A)
Location

Chromosome 5:150860025 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56514338, rs60413553

This variation has 2 HGVS names - click the plus to show

5:g.150860025G>A
ENST00000520549.1:c.158+11371G>A

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

Variation displays