Original source

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

Alleles
CCGCGC/- | MAF: 0.49 (CCGCGC)
Location

Chromosome 5:135028717-135028722 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs145747214

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

Variation displays