Original source

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

Alleles
C/- | Ancestral: C | MAF: 0.11 (-)
Location

Chromosome 4:155210311 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs141933156

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

Variation displays