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: 0.04 (C)
Location

Chromosome 10:82192849 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 8 HGVS names - click the plus to show

10:g.82192849T>C
ENST00000555784.2:c.136-165890T>C
ENST00000602794.2:c.*372-165890T>C
ENST00000404547.2:c.824-165890T>C
ENST00000404576.3:c.235+26023T>C
ENST00000372142.3:c.160+26023T>C
ENST00000556918.2:c.235+26023T>C
ENST00000372141.3:c.824-165890T>C

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

Variation displays