Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


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