Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.49 (T)
Location

Chromosome 19:44905579 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR982405

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs60575746, rs676912

HGVS name

19:g.44905579T>G

This variation has assays on 10 chips - click the plus to show

Variation displays