Original source

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

Alleles
-/A | MAF: 0.26 (A)
Location

Chromosome 12: between 21131687 and 21131688 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs374850048, rs140501804

This variation has 6 HGVS names - click the plus to show

Variation displays