Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.18 (G)
Location

Chromosome 12:13563041 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000012.11:g.13715975A>G

This variation has 2 HGVS names - click the plus to show

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

Variation displays