Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.11 (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

Variation displays