Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.20 (G)
Location

Chromosome 22:41990945 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60800027

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2511 sample genotypes.

Variant displays