Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.12 (T)
Location

Chromosome 9:99147471 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs16918310, rs60400375

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Affy GeneChip 500K

About this variant

This variant overlaps 6 transcripts and has 6046 sample genotypes.

Variant displays