Original source

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

A/T | Ancestral: A | Ambiguity code: W | MAF: 0.29 (T)

Chromosome 1:16996703 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60249437

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GeneChip 500K, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 14 transcripts, has 2782 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays