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 4:154753197 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

4:g.154753197T>C

Genotyping chips

This variant has assays on: Illumina_CytoSNP12v1, Affy GeneChip 500K, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 7 transcripts, has 4162 sample genotypes and is mentioned in 1 citation.

Variant displays