Original source

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

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 10 transcripts, has 3845 sample genotypes and is mentioned in 2 citations.

Variant displays