Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.26 (G)
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60096014, rs60383155

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

18:g.63791454C>G
ENST00000447428.4:c.169-939C>G
ENST00000425392.4:c.169-939C>G
ENST00000431370.1:c.169-939C>G
ENST00000398019.5:c.169-939C>G
ENST00000540675.4:c.169-1707C>G
ENST00000336429.5:c.169-939C>G
ENST00000546027.4:c.169-939C>G

Genotyping chips

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

About this variant

This variant overlaps 7 transcripts, has 2618 individual genotypes and is mentioned in 1 citation.

Variation displays