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: 0.44 (C)
Location

Chromosome 19:17796030 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58123794, rs17750601

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

19:g.17796030C>T
ENST00000600777.1:c.-51+857C>T
ENST00000318683.6:c.-51+824C>T
ENST00000599265.3:c.-51+1147C>T
ENST00000595387.1:c.-70+824C>T

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

Variation displays