Original source

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

Alleles
-/A/C | MAF: 0.17 (C)
Location

Chromosome 12: between 21131693 and 21131694 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs143871795

This variation has 12 HGVS names - click the plus to show

Variation displays