Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

TATGTGTATA/- | MAF: 0.22 (-)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs148784561

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2507 sample genotypes.

Variant displays