Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.05 (C)
Location

Chromosome 10:83655900 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17646354

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

10:g.83655900T>C
ENST00000602794.1:c.*371+6479T>C
ENST00000555784.1:c.135+18049T>C
ENST00000404547.1:c.823+19981T>C
ENST00000404576.2:c.135+18049T>C
ENST00000556918.1:c.135+18049T>C
ENST00000372142.2:c.60+18124T>C
ENST00000372141.2:c.823+19981T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays