Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.44 (T)
Location

Chromosome 6:38398097 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57856129

This variant has 5 HGVS names - click the plus to show

6:g.38398097T>C
ENST00000419706.6:c.1064+4720A>G
ENST00000314100.10:c.951-53004A>G
ENST00000481247.5:c.1155-53004A>G
ENST00000328403.10:c.*63-53004A>G

This variant has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 4 transcripts, has 2515 sample genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variant displays