Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.10 (T)
Location

Chromosome 11:72008357 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs56966640, rs60870026

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 14 transcripts and has 4312 sample genotypes.

Variant displays