Original source

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

Alleles
-/T
Location

Chromosome 12: between 11667696 and 11667697 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs369062019

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

Variation displays