Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

Variant displays