Original source

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

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2507 sample genotypes.

Variant displays