Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (C)
Location

Chromosome 7:39018977 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386606747, rs17255952

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_HumanHap650Y

About this variant

This variant overlaps 3 transcripts and has 3896 individual genotypes.

Variation displays