Original source

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

Alleles
TTTT/-/TTTTT
Location

Chromosome 10:6188850-6188853 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60895048

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

Variation displays