Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.41 (A)
Location

Chromosome 7:93910215 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs61124953, rs10330759

HGVS names

This variant has 4 HGVS names - Show

About this variant

Variant displays