Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.12 (A)
Location

Chromosome 1:12165294 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60883607, rs57909747

HGVS name

1:g.12165294T>A

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 4481 individual genotypes and is mentioned in 5 citations.

Variation displays