Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.29 (T)
Location

Chromosome 10:122455905 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 2 HGVS names - Hide

10:g.122455905C>T
ENST00000528446.1:c.297+881C>T

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 1 transcript, has 3692 sample genotypes, is associated with 4 phenotypes and is mentioned in 11 citations.

Variant displays