Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
TATGTGTATA/- | MAF: 0.22 (-)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs148784561

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

About this variant

This variant overlaps 7 transcripts and has 2507 sample genotypes.

Variant displays