Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.09 (G)
Location

Chromosome 4:73980911 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs1247192, rs57567568

HGVS name

4:g.73980911A>G

About this variant

This variant overlaps 1 transcript and has 2849 sample genotypes.

Variant displays