Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: < 0.01 (T)
Location

Chromosome 4:47029738 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2504 sample genotypes.

Variant displays