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: 0.44 (T)
Location

Chromosome 19:22051986 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs11669276

HGVS name

19:g.22051986T>G

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

Variation displays