Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.02 (T)
Location

Chromosome 15:43063719 (forward strand) | View in location tab

Co-located

with dbSNP rs199666034 (T/C)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57951808, rs56351870

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays