Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.38 (C)
Location

Chromosome 19:50025640 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

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

19:g.50025640C>T
ENST00000599538.2:c.-359G>A
ENST00000596445.2:c.-65+28G>A

This variation has assays on 7 chips - click the plus to show

Variation displays