Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

Synonyms

Archive dbSNP rs386585437, rs58200861

This variation has 2 HGVS names - click the plus to show

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

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

About this variant

This variant overlaps 1 transcript, has 2798 individual genotypes, is associated with 3 phenotypes and is mentioned in 9 citations.

Variation displays