Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]


Chromosome 7: between 128241953 and 128241954 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs113467677, rs28954082

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

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human1M-duo

About this variant

This variant overlaps 2 transcripts and has 46 individual genotypes.

Variation displays