Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 10:81896144 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17646354

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

10:g.81896144T>C
ENST00000555784.5:c.135+18049T>C
ENST00000602794.5:c.*371+6479T>C
ENST00000404576.6:c.135+18049T>C
ENST00000404547.5:c.823+19981T>C
ENST00000372142.6:c.60+18124T>C
ENST00000556918.5:c.135+18049T>C
ENST00000372141.6:c.823+19981T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 7 transcripts, has 2598 sample genotypes and is mentioned in 1 citation.

Variant displays