Original source

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

Alleles
TATT/-|MAF: 0.32 (-)
Location

Chromosome 5:135030019-135030022 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs33953498, rs147022439

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2512 sample genotypes.

Variant displays