Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 19:45305950 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58877977, rs17875632

HGVS name

19:g.45305950T>C

This variant has assays on 8 chips - click the plus to show

About this variant

Variant displays