Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.37 (C)
Location

Chromosome 7:44163407 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61057400, rs17832276

This variant has 4 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 4317 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays