Original source

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

Alleles
-/GGTCT | MAF: 0.01 (GGTCT)
Location

Chromosome 11: between 67364527 and 67364528 (forward strand) | View in location tab

Most severe consequence

This variation has 4 HGVS names - click the plus to show

Variation displays