Original source

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

Alleles
TTT/-/T
Location

Chromosome 10:112957214-112957216 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57636197, rs72192370

This variation has 28 HGVS names - click the plus to show

Variation displays