Original source

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

Alleles
-/TTTT | MAF: 0.29 (-)
Location

Chromosome 12: between 11667532 and 11667533 (forward strand) | View in location tab

Most severe consequence

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

Variation displays