Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.02 (G)
Location

Chromosome 22:33272841 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs73885033

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays