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: 0.40 (C)
Location

Chromosome 6:43997428 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57503978

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

6:g.43997428T>C
ENST00000422059.2:n.647-120A>G
ENST00000607590.1:n.430-120A>G

This variation has assays on 9 chips - click the plus to show

Variation displays