Original source

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

-/TTTG | MAF: 0.44 (TTTG)

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

Most severe consequence
Intron variant
Evidence status


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