Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.10 (G)
Location

Chromosome 22:50584723 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs52814495

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2774 individual genotypes.

Variation displays