Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.21 (T)
Location

Chromosome 9:133635393 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR014914

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60944937

HGVS name

9:g.133635393T>C

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3960 sample genotypes, is associated with 1 phenotype and is mentioned in 53 citations.

Variant displays