Original source

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

Alleles
-/TTTG|MAF: 0.44 (TTTG)
Location

Chromosome 10: between 98475720 and 98475721 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60374450, rs149020554

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2508 sample genotypes.

Variant displays