Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.10 (C)
Location

Chromosome 19:40718299 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS080711

Most severe consequence
Evidence status

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

19:g.40718299G>C
ENST00000263370.2:c.1155+9G>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays