Original source

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

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

Chromosome 4:123395529 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

4:g.123395529A>G

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2758 sample genotypes.

Variant displays