Original source

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

Alleles
TATGTGTATA/- | MAF: 0.27 (-)
Location

Chromosome 10:74017733-74017742 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs148784561

This variation has 7 HGVS names - click the plus to show

Variation displays