Original source

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

Alleles
-/C | MAF: 0.29 (-)
Location

Chromosome 18: between 5408276 and 5408277 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs142726137

This variation has 17 HGVS names - click the plus to show

Variation displays