Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.29 (G)
Location

Chromosome 18:63791454 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 8 HGVS names - Hide

18:g.63791454C>G
ENST00000431370.1:c.169-939C>G
ENST00000425392.5:c.169-939C>G
ENST00000398019.6:c.169-939C>G
ENST00000447428.5:c.169-939C>G
ENST00000540675.5:c.169-1707C>G
ENST00000336429.6:c.169-939C>G
ENST00000546027.5:c.169-939C>G

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Affy GeneChip 500K

About this variant

This variant overlaps 7 transcripts, has 4026 sample genotypes and is mentioned in 1 citation.

Variant displays