Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.11 (T)
Location

Chromosome 1:186671571 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs79035632, rs17581169

HGVS name

1:g.186671571G>T

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 4 transcripts, has 3655 sample genotypes and is mentioned in 3 citations.

Variant displays