Original source

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

Alleles
-/AATG/ATGA
Location

Chromosome 7: between 127882006 and 127882007 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs113467677, rs28954082

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

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad

Variation displays