Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.35 (A)
Location

Chromosome 7:39460922 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs386609852, rs17713083

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

About this variant

This variant overlaps 5 transcripts and has 3765 sample genotypes.

Variant displays