Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (C)
Location

Chromosome 9:73150435 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

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

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays