Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.38 (T)
Location

Chromosome 22:37242920 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59743864

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 3976 sample genotypes and is mentioned in 1 citation.

Variant displays