Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.21 (C)
Location

Chromosome 4:54295646 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3796765, rs58505840

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

This variation has assays on 6 chips - click the plus to show

Variation displays