Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 9:87003113 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60246708

HGVS name

9:g.87003113T>C

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3684 sample genotypes and is mentioned in 1 citation.

Variant displays