Original source

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

Alleles
GTT/- | MAF: 0.11 (-)
Location

Chromosome 15:40722530-40722532 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs374610247

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays