Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.33 (T)
Location

Chromosome 7:147492648 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 3 HGVS names - click the plus to show

7:g.147492648C>T
ENST00000361727.6:c.1777+6607C>T
ENST00000361727.6:c.1777+6607C>T

Genotyping chips

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

About this variant

This variant overlaps 4 transcripts, has 4304 individual genotypes and is mentioned in 3 citations.

Variation displays