Original source

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

Alleles
T/-
Location

Chromosome 15:40724910 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs71104731, rs71428305

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

About this variant

This variant overlaps 7 transcripts and has 2 sample genotypes.

Variant displays