Original source

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

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

Chromosome 12: between 11820466 and 11820467 (forward strand) | View in location tab

Most severe consequence

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

Variation displays