Original source

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

Alleles
T/C/G|Ancestral: T|Ambiguity code: B|MAF: 0.50 (C)
Location

Chromosome 9:101420658 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3174334, rs117863370

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts and has 2777 sample genotypes.

Variant displays