Original source

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

Alleles
TATT/- | MAF: 0.32 (-)
Location

Chromosome 5:135030019-135030022 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs33953498, rs147022439

This variation has 5 HGVS names - click the plus to show

Variation displays