Original source

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

Alleles
-/TTTG
Location

Chromosome 10: between 98475720 and 98475721 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60374450, rs149020554

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

Variation displays