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
ENST00000314100.7:c.951-53004A>G
ENST00000419706.3:c.1064+4720A>G
ENST00000481247.2:c.1155-53004A>G
ENST00000328403.7:c.*63-53004A>G

This variation has assays on 12 chips - click the plus to show

Variation displays