Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.03 (G)
Location

Chromosome 14:21634977 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61971847, rs111195048

HGVS name

14:g.21634977T>G

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 3629 individual genotypes.

Variation displays