Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome 10:83952605 (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.83952605T>C
ENST00000555784.1:c.136-165890T>C
ENST00000602794.1:c.*372-165890T>C
ENST00000404576.2:c.235+26023T>C
ENST00000404547.1:c.824-165890T>C
ENST00000372142.2:c.160+26023T>C
ENST00000556918.1:c.235+26023T>C
ENST00000372141.2:c.824-165890T>C

This variation has assays on 8 chips - click the plus to show

Variation displays