Original source

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

Alleles
-/GGC | MAF: < 0.01 (GGC)
Location

Chromosome 12: between 48766731 and 48766732 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

Variation displays