Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.32 (T)
Location

Chromosome 4:154753197 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

4:g.154753197T>C

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

Variation displays