Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.12 (G)
Location

Chromosome 7:100422481 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1647622

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni2.5

Variation displays