Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.03 (C)
Location

Chromosome 9:101431771 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17187052, rs1634125

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 3232 sample genotypes.

Variant displays