Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.22 (T)
Location

Chromosome 6:20728500 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60110599

This variation has 3 HGVS names - click the plus to show

6:g.20728500T>C
ENST00000274695.5:c.372-11019T>C
ENST00000378610.1:c.372-11019T>C

This variation has assays on 14 chips - click the plus to show

Variation displays