Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.41 (G)
Location

Chromosome 7:93910167 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs60926416, rs10330044

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

This variant has assays on 8 chips - click the plus to show

About this variant

Variant displays