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: 0.39 (C)
Location

Chromosome 3:157080986 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17385692

HGVS name

3:g.157080986T>C

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays