Original source

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

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

Chromosome 18: between 5408275 and 5408276 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs142726137

This variation has 19 HGVS names - click the plus to show

Variation displays