Original source

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

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

Chromosome 1:97078076 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs199469572

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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, has 3005 sample genotypes and is associated with 1 phenotype.

Variant displays