Original source

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

T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.03 (C)

Chromosome 1:150658393 (forward strand) | View in location tab


with dbSNP rs55692553 (C/T)

Most severe consequence
Evidence status


Archive dbSNP rs2867305, rs9436012, rs1707157

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 2 transcripts and has 1893 individual genotypes.

Variation displays