Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.25 (T)
Location

Chromosome 17:7281162 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

17:g.7281162T>C

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 3765 individual genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variation displays