Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.06 (C)
Location

Chromosome 12:53720345 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 21 transcripts and has 3804 sample genotypes.

Variant displays