Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.44 (G)
Location

Chromosome 7:39349348 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 7 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 6 transcripts and has 6248 individual genotypes.

Variation displays