Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2512 sample genotypes.

Variant displays