Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.47 (C)
Location

Chromosome 7:22812880 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58854805

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2513 sample genotypes.

Variant displays