Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.31 (T)
Location

Chromosome 2:102454108 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR084631

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60796178

HGVS name

2:g.102454108T>C

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3886 sample genotypes, is associated with 3 phenotypes and is mentioned in 57 citations.

Variant displays