Original source

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

Alleles
AC/-/CA | MAF: 0.29 (-)
Location

Chromosome 12:11727675-11727676 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

Variation displays