Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (G)
Location

Chromosome 5:150879305 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56583800, rs57988777

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

5:g.150879305A>G
ENST00000520549.1:c.*79-280A>G

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

Variation displays