Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.37 (C)
Location

Chromosome 22:31953076 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56600775, rs60696797

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 6 transcripts, 2 regulatory features, has 3784 sample genotypes and is mentioned in 1 citation.

Variant displays