Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.11 (-)
Location

Chromosome 15:40706105 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs141177078

This variant has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2505 sample genotypes.

Variant displays