Original source

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

This variant has 7 HGVS names - click the plus to show

This variant has assays on 10 chips - click the plus to show

About this variant

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

Variant displays