Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.20 (C)
Location

Chromosome 22:31952326 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17681756

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

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2843 sample genotypes and is mentioned in 1 citation.

Variant displays