Original source

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

TTTAT/- | MAF: 0.28 (TTTAT)

Chromosome 11:120262988-120262992 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs144192477

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2512 sample genotypes.

Variant displays