Original source

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

Alleles
-/T | MAF: 0.48 (T)
Location

Chromosome 11: between 102468725 and 102468726 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138243832, rs59085181

This variation has 3 HGVS names - click the plus to show

Variation displays