Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.35 (C)
Location

Chromosome 3:157080986 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17385692

HGVS name

3:g.157080986T>C

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 2541 individual genotypes, is associated with 2 phenotypes and is mentioned in 9 citations.

Variation displays