Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.22 (C)
Location

Chromosome 9:35074920 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

Archive dbSNP rs17882272

This variant has 8 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 4016 sample genotypes and is mentioned in 1 citation.

Variant displays