Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.47 (G)
Location

Chromosome 22:35072496 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60493943, rs60643890

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_Human660W-quad

About this variant

This variant overlaps 2 transcripts and has 3962 sample genotypes.

Variant displays