Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.32 (T)
Location

Chromosome 7:147491593 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs10373812, rs57823747

This variant has 2 HGVS names - click the plus to show

7:g.147491593G>T
ENST00000361727.7:c.1777+5552G>T

Genotyping chips

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

About this variant

This variant overlaps 1 transcript, has 3657 sample genotypes and is mentioned in 3 citations.

Variant displays