Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 19:41860296 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR993676

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

19:g.41860296A>G
ENST00000604123.1:c.142+76A>G
ENST00000604424.1:n.350+3189A>G
ENST00000539627.1:c.-30+3189A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays