Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61057400, rs17832276

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - 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