Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.47 (T)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57856129

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

6:g.38398097T>C
ENST00000314100.9:c.951-53004A>G
ENST00000419706.5:c.1064+4720A>G
ENST00000481247.4:c.1155-53004A>G
ENST00000328403.9:c.*63-53004A>G

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

About this variant

This variant overlaps 4 transcripts, has 2565 individual genotypes, is associated with 1 phenotype and is mentioned in 8 citations.

Variation displays