Original source

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

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 22:31950775 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60502909

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

About this variant

Variant displays