Original source

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

TATGTGTATA/- | MAF: 0.27 (-)

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

Most severe consequence
Evidence status


Archive dbSNP rs148784561

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 1095 individual genotypes.

Variation displays