Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.27 (T)
Location

Chromosome 1:186671485 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386594400

HGVS name

1:g.186671485C>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts, has 2975 individual genotypes and is mentioned in 4 citations.

Variation displays