Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57856129

HGVS names

This variant has 5 HGVS names - Hide

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

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant overlaps 4 transcripts, has 3968 sample genotypes, is associated with 1 phenotype and is mentioned in 9 citations.

Variant displays