Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 2 HGVS names - Hide

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

Genotyping chips

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

About this variant

This variant overlaps 1 transcript, 2 regulatory features, has 4304 sample genotypes and is mentioned in 3 citations.

Variant displays