This variation maps to 7 locations

Select a location:
Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs192285748

HGVS name

None

Genotyping chips

This variation has assays on: Illumina_Human610_Quad, Illumina_HumanOmni5, Illumina_Human1M-duo

About this variant

This variant overlaps 2 transcripts and has 1334 individual genotypes.

Variation displays