Original source

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

Alleles
C/A | Ambiguity code: M | MAF: 0.28 (A)
Location

Chromosome 10:133533423 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57034966

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

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2921 sample genotypes and is mentioned in 2 citations.

Variant displays