Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.34 (T)
Location

Chromosome 12:90963572 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58781624, rs17251134

HGVS name

12:g.90963572T>G

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

Variation displays