Original source

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

Alleles
-/T/TT
Location

Chromosome 6: between 111602319 and 111602320 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58964142, rs199701039

This variation has 12 HGVS names - click the plus to show

Variation displays