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 (C)
Location

Chromosome 17:34358987 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs56522587, rs59584284

HGVS name

17:g.34358987T>C

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 3580 sample genotypes.

Variant displays