Original source

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

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2505 sample genotypes.

Variant displays