Original source

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

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

Chromosome 19:45408836 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR982405

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60575746, rs676912

HGVS name

19:g.45408836T>G

This variation has assays on 9 chips - click the plus to show

Variation displays