Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.10 (T)
Location

Chromosome 10:103954641 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs57190459

HGVS name

10:g.103954641C>T

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant has 3954 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays